CAS No.100-61-8,N-Methylaniline Suppliers,MSDS download

Simagchem Corporation

We have developed techincal-bond fuel additives like as Octane booster and Cetane improver, like N-Methylaniline ,Cyclopentadienyl Manganese Tricarbonyl (CMT) and 2-Ethylhexyl Nitrate; also Pour Point Depressant like 2-Methoxyethanol, to the Eas

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Changzhou Baolong Chemical Industrial Co.,Ltd

We are specialized in producing N-methylaniline (cas#100-61-8) with monthly capacity of 10,000 tons. NMA is our sole product so we guarantee the quality is stable. We export a lot to foreign countries and gained a good reputation among customers

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Aecochem Corp.

Items Specification Appearance Light yellow to red brown liquid Relative density 0.987-0.994 Assay

Supply high quality N-Methylaniline

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Chongqing Changfeng Chemical Co., Ltd.

Chongqing Changfeng Chemical Co., Ltd. is a leading manufacturer of N-methyl aniline in China. As a state-owned company, our annual capacity of this product is around 20,000 metric tons. We are dedicated to offer our best service to our customer

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Xiamen AmoyChem Co.,Ltd

Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi

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Dayang Chem (Hangzhou) Co.,Ltd.

Dayangchem’s R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantiti

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Kono Chem Co.,Ltd

N-Methylaniline/ 100-61-8 1, Specification of N-Methylaniline/ 100-61-8 Item Specifications Result

CAS:100-61-8 N-Methylaniline

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Jinan Finer Chemical Co., Ltd

Product Description Product name N-Methylaniline CAS 100-61-8 Assay 99% Appearance Yellow clear liquid Capacity 500mt/year Min.package 100gram Standard enterpri

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Hefei TNJ chemical industry co.,ltd

Company Name: Hefei TNJ Chemical Industry Co.,Ltd. Registered Address: B911 Xincheng Business Center,South of Dongliu Road, Zhengwu District, Hefei, Anhui,China

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EAST CHEMSOURCES LIMITED

Monomethylaniline Molecular formula: C7H9N Molecular weight: 107.1531 InChI: InChI=1/C7H9N/c1-6-4-2-3-5-7 (6) 8/h2-5H, 8H2,1H3 Molecular structure: Density: 0.992g/cm3 Melting point: -57 C Boiling point: 200.4 C at 760 mmHg Flash point:

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Ality Chemical Corporation

The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi

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Henan Allgreen Chemical Co.,Ltd

high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai

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Hebei yanxi chemical co.,LTD.

hebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm

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Chemwill Asia Co., Ltd.

Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block

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Henan Tianfu Chemical Co., Ltd.

Product Name: N-Methylaniline Synonyms: MONOMETHYLANILINE;N-METHYLANILINE;N-METHYLAMINOBENZENE;N-MONOMETHYLANILINE;(Methylamino)benzene;Benzenamine, N-methyl-;Benzenenamine, N-methyl-;methylaniline(non-specificname) CAS: 100-61-8

100-61-8 MONOMETHYLANILINE

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Henan Sinotech Import&Export Corporation

Chemical Name: N-methyl aniline Synonym: Monomethylaniline; NMA; N-Methylbenzeneamine; (Methylamino)benzene CAS NO.: 100-61-8 Molecular Formula: C6H5-NH-CH3 Properties: NMA is inflammable and explosive in case of direct fire, high temperatu

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Baoji Guokang Healthchem co.,ltd

About us Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad.

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Changchun Artel lmport and Export trade company

Product Detail Minimum Order Qty. 10 Gram

N-Methylaniline CAS NO.100-61-8

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Wuhan Zenuo Biological Medicine Technology Co Ltd

N-Methylaniline big supplier with lower price

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Hangzhou Keyingchem Co.,Ltd

Hangzhou Keying Chem Co., Ltd. Is a comprehensive enterprise, dedicated to the development, production and marketing of chemicals. As a technology innovative and service professional enterprise, Our company mainly engages in global pharmaceutical,

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Triumph International Development Limilted

Triumph has the complete production of G- KG - MT service chain,we can make the new technology into productivity quickly in the research and development of new products. Main Service 1.Own made fine chemical products 2.Out sourcing and quality c

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Hangzhou ZeErRui Chemical Co., Ltd.

hangzhou zeerrui chemical co., ltd. located in lingang industrial areas, our plant covers an area of 6000 square meters.zeerrui dedicated to the development, production and marketing of chemicals. we have earned ourselves a good reputation at home

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Hangzhou J&H Chemical Co., Ltd.

J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia

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Afine Chemicals Limited

Our Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter

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Zibo Hangyu Biotechnology Development Co., Ltd

Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi

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Hangzhou Lingrui Chemical Co.,Ltd.

N-MethylanilineAppearance:Colorless to pale yellow liquid Storage:Stored in a clean,cool, dry area;keep away frommoisture and stong,direct light/heat. Package:according to customers' requirements Application:Used for Synthesis of heterocycle and impo

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Siwei Development Group Ltd.

Product name: N-Methylaniline CAS No.：100-61-8 Molecule Formula：C7H9N Molecule Weight：107.15 Purity: 99.0% Package: 200kg/drum Description：Colorless to light yellow liquid Manufacture Standards：Enterprise Standard

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Zibo Dorne chemical technology co. LTD

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Henan Wentao Chemical Product Co., Ltd.

We are leading fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...)

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Hangzhou Zhongqi chem Co.,Ltd.

Located in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service an

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Synthetic route

: 614-30-2
N-methyl-N-phenyl-benzenemethanamine

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With palladium 10% on activated carbon; hydrogen In methanol at 20℃; for 1.5h;	100%
With hydrogenchloride; hydrogen; palladium on activated charcoal In methanol for 0.25h; Product distribution; Hydrogenolysis;	91%
With sulfuric acid; nickel In methanol; water at 40℃; for 2h;	84%
With triethylsilane; potassium tert-butylate at 130℃; for 18h; Sealed tube; Inert atmosphere;	65%
With titanium(III) chloride; lithium In tetrahydrofuran for 22h; Heating;	55%

: 86518-04-9
1-tert-butyl-N,1,1-trimethyl-N-phenylsilanamine

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With silica gel In ethanol; water at 20℃; for 2h;	100%

: 591-50-4
iodobenzene

: 74-89-5
methylamine

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With copper In water at 100℃; for 12h; Ullmann reaction;	99.8%
With copper(l) iodide; 6,7-dihydro-5H-quinolin-8-one oxime; potassium hydroxide In water at 25℃; for 24h; Inert atmosphere;	95%
With potassium hydroxide In N,N-dimethyl-formamide at 110℃; for 24h; Buchwald-Hartwig Coupling;	65%
With Cu2O nanoparticles (Cu2O-NPs) synthesized in n-Bu4POAc from CuCO3 In water at 75℃; for 16h; Concentration; Ionic liquid;	65 %Spectr.
With copper In water at 100℃; for 24h; Sealed tube;

: 108-86-1
bromobenzene

: 74-89-5
methylamine

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With copper In water at 100℃; for 12h; Ullmann reaction;	99.6%
With potassium hydroxide In N,N-dimethyl-formamide at 110℃; for 20h; Buchwald-Hartwig Coupling;	52%
With tetrakis(triphenylphosphine) palladium(0); caesium carbonate; triphenylphosphine In o-xylene at 160℃; for 12h; Inert atmosphere;

: 67-56-1
methanol

: 62-53-3
aniline

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With C21H36BrMnNO2P2; potassium tert-butylate at 100℃; for 24h; Catalytic behavior; Reagent/catalyst; Time;	99%
With cesiumhydroxide monohydrate; (1,4-dimethyl-5,7-diphenyl-1,2,3,4-tetrahydro-6H-cyclopenta[b]pyrazin-6-one) irontricarbonyl complex3 at 110℃; Schlenk technique; Inert atmosphere;	99%
With C31H30ClIrN3O(1+)*F6P(1-); potassium tert-butylate at 130℃; for 12h; Catalytic behavior; Reagent/catalyst; Temperature;	99%

: 1934-92-5
N-methyl-N-phenyl-benzamide

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With triethyl borane; Triethoxysilane; sodium hydroxide In hexane at 80℃; for 6h; Solvent; Reagent/catalyst; Inert atmosphere; Sealed tube;	99%
With sodium triethylborohydride In tetrahydrofuran at 80℃; for 6h; Inert atmosphere; Schlenk technique; High pressure; Sealed tube;	97%
Multi-step reaction with 3 steps 1: 48 percent / P2S5 / dioxane / 2 h / Ambient temperature 2: tetrahydrofuran / Ambient temperature 3: 44 percent Spectr. / NaBH4, ZnCl2 / methanol / 2 h View Scheme
With C18H37ClMoNO2P2; hydrogen; sodium triethylborohydride In tetrahydrofuran; toluene at 100℃; under 37503.8 Torr; for 24h; Autoclave; Glovebox;	28 %Chromat.

: 124-38-9
carbon dioxide

: 1145-27-3
N,N’-dimethyl-N,N’-diphenylmethanediamine

A: 121-69-7
N,N-dimethyl-aniline

B: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With diphenylsilane; cesium formate In acetonitrile at 50℃; under 750.075 Torr; Green chemistry;	A 99% B n/a

...Expand

: 55577-65-6
2,N-dimethyl-N-phenylpropanamide

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With triethyl borane; Triethoxysilane; sodium hydroxide In hexane at 80℃; for 6h; Solvent; Reagent/catalyst; Inert atmosphere; Sealed tube;	99%
With sodium triethylborohydride In tetrahydrofuran at 80℃; for 6h; Inert atmosphere; Schlenk technique; High pressure; Sealed tube;	88%

: 5827-78-1
N-methyl-N-phenylpropanamide

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With triethyl borane; Triethoxysilane; sodium hydroxide In hexane at 80℃; for 6h; Inert atmosphere; Sealed tube;	99%
With sodium triethylborohydride In tetrahydrofuran at 80℃; for 6h; Inert atmosphere; Schlenk technique; High pressure; Sealed tube;	94%

: 618-40-6
1-Methyl-1-phenylhydrazine

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With hydrogen; lithium 1-naphthalenide; nickel dichloride In tetrahydrofuran at 20℃; under 760.051 Torr; for 1h;	98%
With titanium(III) chloride; water In tetrahydrofuran pH=7; Reflux; Alkaline aq. solution; Inert atmosphere;	83%
With Wilkinson's catalyst In methanol at 25℃; for 24h;	80%

: 93-61-8
N-methyl-N-phenylformamide

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With 1,3-Dimethoxybenzene; trichlorophosphate In dichloromethane at 40℃; for 24h; Product distribution; other carboxamides, var. solvents, var. temp., var. time, var. reagents mole ratio;	97%
With C18H37ClMoNO2P2; hydrogen; sodium triethylborohydride In tetrahydrofuran; toluene at 100℃; under 37503.8 Torr; for 24h; Catalytic behavior; Reagent/catalyst; Solvent; Pressure; Temperature; Autoclave; Glovebox;	94%
With aluminum oxide; potassium fluoride for 0.333333h; microwave irradiation;	80%

: 5827-78-1
N-methyl-N-phenylpropanamide

A: 13395-54-5
N-methyl-N-n-propylaniline

B: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With triethyl borane; sodium hydroxide In hexane at 80℃; for 6h; Inert atmosphere; Sealed tube;	A 1% B 97%

: 579-10-2
N-acetyl-N-methylaniline

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With 40% potassium fluoride/alumina at 85℃; for 0.0666667h; Microwave irradiation; Neat (no solvent);	96%
With 9,10-dihydroanthracene; sodium triethylborohydride In tetrahydrofuran at 80℃; for 6h; Solvent; Reagent/catalyst; Inert atmosphere; Schlenk technique; High pressure; Sealed tube;	86%
With [RuCl2(2-(diphenylphosphino)-N-((6-((diphenylphosphino)methyl)pyridin-2-yl)methyl)ethan-1-amine)]; potassium tert-butylate; hydrogen In tetrahydrofuran at 100℃; under 37503.8 Torr; for 20h; Catalytic behavior; Autoclave; chemoselective reaction;	85%

: 108-90-7
chlorobenzene

: 74-89-5
methylamine

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With C38H49N2P*C9H10ClPd In 1,4-dioxane at 20℃; for 18h; Inert atmosphere; Schlenk technique;	96%
With potassium hydroxide In N,N-dimethyl-formamide at 110℃; for 24h; Buchwald-Hartwig Coupling;	45%
With water; copper(l) chloride at 220℃;

: 614-00-6
N-methyl-N-nitrosoaniline

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With triethylsilane; hydrogen iodide In dichloromethane at 20℃; for 0.25h; Reagent/catalyst;	95%
With sodium tetrahydroborate; titanium tetrachloride In 1,2-dimethoxyethane for 14h; Ambient temperature;	92%
With iron; acetic acid

: 28685-60-1
N-carbomethoxy-N-methylaniline

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With methyllithium; lithium bromide In tetrahydrofuran at 0℃; for 1h;	95%
With sodium hydrogen telluride In N,N-dimethyl-formamide at 70 - 75℃; for 5h;	82%
With Benzeneselenol; sodium hydride 1.) THF, 2.) HMPA, 10 h, reflux; Yield given. Multistep reaction;

: 109-73-9
N-butylamine

: 3-methyl-2-(N-methylanilino)benzothiazolium toluene-p-sulphonate

A: 70038-63-0
butyl-(3-methyl-3H-benzothiazol-2-ylidene)-amine

B: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
In dichloromethane at 25℃; for 3h;	A 95% B 88%
at 25℃; for 3h;	A 95% B 88%

...Expand

: Indazol-1-ylmethyl-phenyl-amine

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In diethyl ether at 25℃; for 5h; var. aminals deriv. of hydroxymethylindazole;	95%

: 90-10-8
N-methylbenzenesulfonanilide

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; potassium tert-butylate In dimethyl sulfoxide at 20℃; for 17h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Irradiation; Sealed tube;	95%
With trimethylsilyl iodide In acetonitrile at 82℃; for 12h;	91%
With chloro-trimethyl-silane; sodium iodide In acetonitrile for 3h; Heating;	86%

: C20H20N2O4

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With benzyltriethylammonium tetrathiomolybdate In acetonitrile at 28℃; for 0.5h;	95%

: 50-00-0
formaldehyd

: 62-53-3
aniline

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With butyl triphenylphosphonium tetraborate at 20℃; for 0.25h;	94%
With (CuAl)O(x); hydrogen In tetrahydrofuran at 120℃; under 3750.38 Torr; for 9h; Catalytic behavior; Reagent/catalyst; Solvent;	89%
With hydrogen In 1,4-dioxane at 60℃; under 7500.75 Torr; for 24h; Autoclave;	88%

: 2621-79-6
ethyl N-methyl-N-phenylcarbamate

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With methyllithium; lithium bromide In tetrahydrofuran at 0℃; for 1h;	94%

: 121-69-7
N,N-dimethyl-aniline

A: 50-00-0
formaldehyd

B: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With {Ru(IV)O(2,2`-bipyridine)(PPh3)}(ClO4)2 In acetonitrile at 21℃; Rate constant; Kinetics; Thermodynamic data; other Ru(IV) complex catalyst, ΔH(excit), ΔS(excit) determined;	A n/a B 94%
With dihydrogen peroxide; FePp In ethanol at 38℃; for 0.166667h; Product distribution; borate buffer, pH 9; further educts;
With phosphate buffer; dihydrogen peroxide; cytochrome c at 30℃; Equilibrium constant; Rate constant; also in the presence of phosphate bilayer;

: N-methyl-N-tritylaniline

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
Stage #1: N-methyl-N-tritylaniline With naphthalene; lithium In tetrahydrofuran at 0℃; for 1h; Stage #2: With water In tetrahydrofuran at 0 - 20℃;	94%

: 618-40-6
1-Methyl-1-phenylhydrazine

: 135-19-3
β-naphthol

A: 2834-92-6
1-amino-2-naphthol

B: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
In ethylene glycol at 80℃; Solvent; Temperature; Inert atmosphere; regioselective reaction;	A 88% B 94%
at 80℃; for 4h;	A 0.43 g B 0.50 g

...Expand

: {Ru(IV)O(2,2`-bipyridine)(PPh3)}(ClO4)2

: 121-69-7
N,N-dimethyl-aniline

A: 512844-06-3
{Ru(2,2'-bipyridine)2(NCMe)(PPPh3)}(2+)

B: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
In acetonitrile Kinetics; byproducts: CH2O; stoicheiometric oxidation of N,N-dimethylaniline by the Ru complex in MeCN at 21°C; spectrophotometrical determination of the rate constant;	A n/a B 94%

...Expand

: 103-84-4
Acetanilid

: 77-78-1
dimethyl sulfate

A: 579-10-2
N-acetyl-N-methylaniline

B: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With hexamethylenetetramine hydrobromide; potassium carbonate In benzene at 8 - 10℃; for 0.75h;	A 93% B n/a

...Expand

: 64999-94-6
N-methyl-N-phenyl-4-nitrobenzene sulphonamide

: 68-11-1
mercaptoacetic acid

A: 3406-75-5
2-(4-nitrophenylthio)acetic acid

B: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 20℃;	A n/a B 93%

...Expand

: 62-53-3
aniline

: 74-88-4
methyl iodide

: 100-61-8
N-methylaniline

Conditions

Conditions	Yield
With C24H52B20Cl2Rh2Se2 In toluene at 20℃; for 1.66667h;	93%
Stage #1: aniline With n-butyllithium In tetrahydrofuran; hexane at -40℃; for 0.25h; Inert atmosphere; Stage #2: methyl iodide In tetrahydrofuran; hexane at -60 - 20℃; for 8h; Inert atmosphere;
With potassium carbonate In N,N-dimethyl-formamide at 55℃; for 24h; Sealed tube;

: 556-52-5
oxiranyl-methanol

: 100-61-8
N-methylaniline

: 42871-95-4
3-(methyl(phenyl)amino)propane-1,2-diol

Conditions

Conditions	Yield
In methanol for 48h; Reflux;	100%
In ethanol at 120℃; for 0.333333h; Microwave irradiation;	81%

: 102-92-1
cinnamoyl chloride

: 100-61-8
N-methylaniline

: 27687-46-3
N-methyl-N-phenylcinnamamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 20℃; Inert atmosphere;	100%
In dichloromethane at 20℃; for 1h;	97%
With triethylamine In ethyl acetate at 0 - 20℃;	79%

: 622-78-6
Benzyl isothiocyanate

: 100-61-8
N-methylaniline

: 70741-04-7
N'-benzyl-N-methyl-N-phenyl-thiourea

Conditions

Conditions	Yield
In ethanol at 25 - 30℃; for 1h;	100%
With ethanol

: 103-72-0
phenyl isothiocyanate

: 100-61-8
N-methylaniline

: 4949-93-3
1-methyl-1,3-diphenyl-thiourea

Conditions

Conditions	Yield
In ethanol at 25 - 30℃; for 1h;	100%
Wavelength; Reagent/catalyst; Darkness;	97%
In ethanol for 0.166667h; Heating;	60%

: 4755-77-5
Ethyl oxalyl chloride

: 100-61-8
N-methylaniline

: 1457-86-9
ethyl-2-(methyl(phenyl)amino)-2-oxoacetate

Conditions

Conditions	Yield
With triethylamine In dichloromethane for 0.5h; Ambient temperature;	100%
With triethylamine In dichloromethane at 0 - 20℃;	85%
With pyridine
With pyridine In dichloromethane for 5h; Ambient temperature;

: 107-13-1
acrylonitrile

: 100-61-8
N-methylaniline

: 94-34-8
N-(2-cyanoethyl)-N-methylaniline

Conditions

Conditions	Yield
With 1,1,1,3',3',3'-hexafluoro-propanol at 20℃; under 10501100 Torr; for 17h; Michael Addition;	100%
With Ps-AlCl3 at 70℃; for 3h; Michael Addition; chemoselective reaction;	99%
With SBA-15-supported Co(II) complex at 20℃; for 3h; Michael condensation;	82%

: 598-21-0
2-Bromoacetyl bromide

: 100-61-8
N-methylaniline

: 29182-97-6
N-methyl-2-bromoacetanilide

Conditions

Conditions	Yield
With triethylamine In ethyl acetate at 0 - 25℃; for 0.5h;	100%
In dichloromethane at 0 - 20℃; for 1h;	98%
With triethylamine In dichloromethane at 20℃; for 16h;	88%

: 2284-20-0
4-Methoxyphenyl isothiocyanate

: 100-61-8
N-methylaniline

: N'-(4-methoxy-phenyl)-N-methyl-N-phenyl-thiourea

Conditions

Conditions	Yield
In ethanol at 25 - 30℃; for 1h;	100%

: 88-88-0
2,4,6-trinitrochlorobenzene

: 100-61-8
N-methylaniline

: 56042-31-0
N-methyl-2,4,6-trinitrodiphenylamine

Conditions

Conditions	Yield
In acetonitrile at 25℃;	100%
With ethanol
With ethanol; sodium acetate

: 109-69-3
n-Butyl chloride

: 100-61-8
N-methylaniline

: 3416-49-7
N-butyl-N-methylaniline

Conditions

Conditions	Yield
With 3-(2-ethoxy-2-oxoethyl)-1-methyl-1H-imidazol-3-ium chloride at 90℃; for 3h; Inert atmosphere; Green chemistry;	100%

: 100-61-8
N-methylaniline

: 614-69-7
2-tolyl isothiocyanate

: N-methyl-N-phenyl-N'-o-tolyl-thiourea

Conditions

Conditions	Yield
In ethanol at 25 - 30℃; for 1h;	100%

: 100-61-8
N-methylaniline

: 1985-12-2
4-Bromophenyl isothiocyanate

: 107775-44-0
N-methyl-N-phenyl-N'-p-bromophenylthiourea

Conditions

Conditions	Yield
In ethanol at 25 - 30℃; for 1h;	100%

: 100-61-8
N-methylaniline

: 614-00-6
N-methyl-N-nitrosoaniline

Conditions

Conditions	Yield
With oxygen; nitrogen(II) oxide In 1,2-dichloro-ethane for 24h; Product distribution; Mechanism; Ambient temperature; other amines, other solvents, var. time;	100%
With oxygen; nitrogen(II) oxide In 1,2-dichloro-ethane for 24h; Ambient temperature;	100%
With toluene-4-sulfonic acid; methoxybenzene; sodium nitrite In dichloromethane at 20℃; chemoselective reaction;	100%

: 762-42-5
dimethyl acetylenedicarboxylate

: 100-61-8
N-methylaniline

: 125735-97-9
2-(methylphenylamino)but-2-enedioic acid dimethyl ester

Conditions

Conditions	Yield
In water at 20℃; for 2h; Michael-type addition;	100%
In water at 20℃;	71%
In water at 0 - 20℃; for 2h;	69%
In diethyl ether

: 100-52-7
benzaldehyde

: 100-61-8
N-methylaniline

: 614-30-2
N-methyl-N-phenyl-benzenemethanamine

Conditions

Conditions	Yield
With sodium tris(acetoxy)borohydride In 1,2-dichloro-ethane at 18℃; for 4h; Solvent; Reagent/catalyst; Green chemistry;	100%
With hydrogen In toluene at 140℃; under 22502.3 Torr; for 18h;	98%
With sodium tetrahydroborate at 20℃; for 0.0333333h; Neat (no solvent); grinding;	97%

: 10242-31-6
1-(4-nitrophenoxy)-2,4,6-trinitrobenzene

: 100-61-8
N-methylaniline

: 56042-31-0
N-methyl-2,4,6-trinitrodiphenylamine

Conditions

Conditions	Yield
In [D3]acetonitrile at 25℃;	100%
In benzene at 30℃;
In benzene at 30℃; Mechanism; Rate constant; various concentrations of N-methylaniline;
In acetonitrile at 25℃; Kinetics; Further Variations:; Solvents;
In [D3]acetonitrile at 25℃; Kinetics; Further Variations:; Solvents;

: 33842-02-3, 529510-96-1
dichloromethylenedimethyliminium chloride

: 100-61-8
N-methylaniline

: 341029-31-0
N,N,N'-Trimethyl-N'-phenyl-carbamidchlorid

Conditions

Conditions	Yield
In dichloromethane	100%

: 1,5-diethoxy-1,5-diphenylpenta-2,4-dienylium perchlorate

: 100-61-8
N-methylaniline

: 1,5-di(N-methyl-N-phenylamino)-1,5-diphenylpenta-2,4-dienylium perchlorate

Conditions

Conditions	Yield
for 0.166667h;	100%

: 1,3,4,6-tetrakis(isopropylthio)thieno<3,4-c>thiophenium bis(tetrafluoroborate)

: 100-61-8
N-methylaniline

: N-<(isopropylthio)-<2,5-bis(isopropylthio)-4-isopropylthio(thiocarbonyl)-3-thienyl>methylene>-N-methyl-N-phenylammonium tetrafluoroborate

Conditions

Conditions	Yield
In acetonitrile at -30℃; for 0.5h;	100%

: 100-61-8
N-methylaniline

: 22696-39-5
N-hydroxy-N-methylaniline

Conditions

Conditions	Yield
With 4-hydroperoxy-5-ethyl-3-methyllumiflavine In tert-butyl alcohol at 30℃; Rate constant;	100%
With sodium perborate; Dihydrate sodium molybdate In acetic acid at 50℃; for 1h; Kinetics; Thermodynamic data; Catalytic behavior; Temperature;	71%
With α-D-glucose 6-phosphate; oxygen; NADP; cyclohexanone monooxygenase at 25℃; for 24h; pH=8.6; Enzymatic reaction;
With air; cyclohexanone monooxygenase from Escherichia coli; NADPH In water at 25℃; pH=8.6; Enzyme kinetics;
With α-D-glucose 6-phosphate; cyclohexanone monooxygenase from Escherichia coli; NADP; glucose-6-phosphate dehydrogenase; air In water at 25℃; for 24h; pH=8.6;

: 22128-62-7
carbonochloridic acid, chloromethyl ester

: 100-61-8
N-methylaniline

: 186353-05-9
[N-methyl-N-phenyl]carbamic acid chloromethyl ester

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃;	100%
With triethylamine In dichloromethane at 0 - 5℃; for 4h;	73%

: 106-43-4
para-chlorotoluene

: 100-61-8
N-methylaniline

: 38158-65-5
N,4-dimethyl-N-phenylaniline

Conditions

Conditions	Yield
With johnphos; sodium t-butanolate; palladium diacetate In toluene at 20℃; for 19h; Arylation;	100%
With potassium tert-butylate; Pd(0) N-heterocyclic carbene-phosphine In 1,4-dioxane at 100℃;	99%
With potassium hydroxide; bis(tri-tert-butylphosphine)palladium(0); cetyltrimethylammonim bromide In water; toluene at 90℃; for 19h;	99%

: 100-61-8
N-methylaniline

: 287721-05-5
4-[phenyl(endo-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)amino]benzoic acid

: N-methyl-4-[(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-phenyl-amino]-N-phenyl-benzamide

Conditions

Conditions	Yield
With N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate Acylation;	100%

: 2845-89-8
1-chloro-3-methoxy-benzene

: 100-61-8
N-methylaniline

: 3-methoxy-N-methyl-N-phenyl-benzenamine

Conditions

Conditions	Yield
With 2'-dicyclohexylphosphanyl-6-methoxy-biphenyl-3-sulfonic acid; palladium diacetate; sodium t-butanolate In diethylene glycol dimethyl ether at 120℃; for 72h; Buchwald-Hartwig Coupling; Inert atmosphere;	100%
With sodium t-butanolate; palladium diacetate In toluene at 80℃; for 1h; Buchwald-Hartwig amination;	97%
With potassium tert-butylate; C36H43Cl2N3OPd In toluene at 130℃; for 12h; Buchwald-Hartwig Coupling; Inert atmosphere; Schlenk technique;	96%

: 100-61-8
N-methylaniline

: 5-bromo-10,20-diphenylporphyrinatonickel(II)

: C39H27N5(2-)*Ni(2+)

Conditions

Conditions	Yield
With 18-crown-6 ether; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; palladium diacetate In tetrahydrofuran at 68℃; for 3h;	100%