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
Cas:75-64-9
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
Cas:75-64-9
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inquirytert-Butylamine Product Name: tert-Butylamine Molecular Weight: 73.13 CAS NO: 75-64-9 EC NO: -- Molecular Formula: C4H11N
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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TIANFUCHEM--75-64-9--High purity tert-Butylamine in stock Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established stable business r
Cas:75-64-9
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inquiryProduct name tert-Butylamine Synonyms 2-AMINOISOBUTANE;2-AMINO-2-METHYLPROPANE;2-METHYL-2-PROPYLAMINE;1 1-Dimethylethylamine;AKOS BBS-00004218;LABOTEST-BB LT01409645;T-BUTYLAMINE;TERT-BUTYLAMINE
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. At p
Cas:75-64-9
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inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:75-64-9
Min.Order:10 Gram
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Type:Trading Company
inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Appearance:white or light yellow crystalline powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:By
Cas:75-64-9
Min.Order:100 Gram
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
Cas:75-64-9
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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
Cas:75-64-9
Min.Order:4 Kilogram
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inquiryJ&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
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
Cas:75-64-9
Min.Order:10 Gram
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inquirySuperior quality Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used in synthetic rubber accelerator, pesticide, med
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
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
stable supply&competitive price Storage:Available Package:25KG Or as client requirement Application:Important pharm intermediate Transportation:By air or By sea
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
Appearance:white powder Storage:tightly from light Package:200kg/drum Transportation:SEA Port:Qingdao
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Hunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:75-64-9
Min.Order:1 Kilogram
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Type:Trading Company
inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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75-64-9 tert-Butylamine Application:75-64-9 tert-Butylamine
1,3,5,7-Tetra-tert-butyl-2,4,6,8-tetrachloro-[1,3,5,7,2,4,6,8]tetrazatetraborocane
A
boric acid
B
tert-butylamine
Conditions | Yield |
---|---|
With water In further solvent(s) byproducts: HCl; solvent cyclohexanol, in tube 20.5 h at 160°C; | A n/a B 97% |
With H2O In further solvent(s) byproducts: HCl; solvent cyclohexanol, in tube 20.5 h at 160°C; | A n/a B 97% |
With water In xylene byproducts: HCl; in tube 20.5 h boiling; | A n/a B 62% |
With H2O In xylene byproducts: HCl; in tube 20.5 h boiling; | A n/a B 62% |
Conditions | Yield |
---|---|
With [Zn(BH4)2(py)] In tetrahydrofuran for 0.67h; Heating; | 96% |
Stage #1: 2-Methyl-2-nitropropane In water; acetonitrile at 20℃; for 0.0833333h; Stage #2: With sodium tetrahydroborate In water; acetonitrile at 20℃; for 0.5h; | 90% |
With palladium on activated charcoal; tetrabutylammomium bromide; water; sodium hydroxide; silicon at 100℃; for 6h; | 86% |
Conditions | Yield |
---|---|
With calcium hydroxide at 240 - 270℃; for 1.5h; other hydroxides as reagent;; | 96% |
With sodium hydroxide In 2-ethoxy-ethanol; water at 100℃; Kinetics; Rate constant; other temperature; activaction energy; | 93% |
Hydrolysis; | 83% |
With sodium hydroxide; ethylene glycol | |
With 2-ethoxy-ethanol; sodium hydroxide |
n-Octylamine
1,4-di-tert-butyl-1,4-diazabutadiene
B
tert-butylamine
Conditions | Yield |
---|---|
With formic acid In water; acetonitrile at 15℃; for 30h; | A 92% B n/a |
Conditions | Yield |
---|---|
at 200 - 230℃; for 0.0833333h; Product distribution; pyrolysis without solvent, product isolated as hydrochloride; | A n/a B 86% |
1,4-di-tert-butyl-1,4-diazabutadiene
1,2-phenylenediacetonitrile
A
naphthalene-1,4-dicarbonitrile
B
tert-butylamine
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 120℃; for 1h; | A 82% B n/a |
Conditions | Yield |
---|---|
With 5-methyl-1,3,4-thiadiazol-2-amine; triethylamine In ethanol; water at 25℃; for 1h; | 81% |
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Schlenk technique; Heating; chemoselective reaction; | A 80% B n/a C n/a |
tert-butylisonitrile
propan-1-ol-3-amine
A
5,6-dihydro-4H-[1,3]oxazine
B
tert-butylamine
Conditions | Yield |
---|---|
With silver cyanide at 90℃; for 18h; | A 70% B n/a |
N-(3-phenylprop-2-yn-1-ylidene)-t-butylamine
4,5-Dimethyl-2(2H)-imidazolinethione
B
tert-butylamine
Conditions | Yield |
---|---|
Stage #1: N-(3-phenylprop-2-yn-1-ylidene)-t-butylamine; 4,5-Dimethyl-2(2H)-imidazolinethione In methanol at 60℃; for 0.5h; Stage #2: With water In methanol | A 70% B n/a |
tert-butyl-(di-tert-butyl-diaziridin-3-ylidene)-amine
A
1,2,4-tri(tert-butyl)semicarbazide
B
1,2-di-tert-butylhydrazine
C
tert-butylamine
D
Tert-butyl isocyanate
Conditions | Yield |
---|---|
With water In 1,4-dioxane for 2h; Reflux; | A 69% B n/a C n/a D n/a |
N-(3-phenylprop-2-yn-1-ylidene)-t-butylamine
4,5-diphenyl-1H-imidazole-2-thiol
B
tert-butylamine
Conditions | Yield |
---|---|
Stage #1: N-(3-phenylprop-2-yn-1-ylidene)-t-butylamine; 4,5-diphenyl-1H-imidazole-2-thiol In methanol at 60℃; for 0.5h; Stage #2: With water In methanol | A 65% B n/a |
3-tert-Butylamino-3-methyl-1-butyne
A
3-tert-Butylamino-tert-pentylamine
B
3-tert-Butylamino-3-methyl-1-butene
C
tert-butylamine
Conditions | Yield |
---|---|
With hydrogen; Lindlar's catalyst In various solvent(s) at -10℃; under 2585.74 Torr; Catalytic hydrogenation; Hydrogenolysis; | A n/a B 64% C n/a |
With hydrogen; W-2 Raney nickel In ethanol Product distribution; Further Variations:; Catalysts; Solvents; Catalytic hydrogenation; Hydrogenolysis; |
A
1,3-di-tert-butylurea
B
N-(pyridin-2-yl)thiophene-3-carboxamide
C
tert-butylamine
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Schlenk technique; Heating; chemoselective reaction; | A n/a B 63% C n/a |
1,4-di-tert-butyl-1,4-diazabutadiene
N-butylamine
A
butyl[2-(butylimino)ethylidene]amine
B
tert-butylamine
Conditions | Yield |
---|---|
With formic acid In water; acetonitrile at 15℃; for 2h; | A 62% B n/a |
2-(3-Bromophenyl)-N-(tert-butyl)imidazo[1,2-a]pyridin-3-amine
A
1,3-di-tert-butylurea
B
tert-butylamine
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Schlenk technique; Heating; chemoselective reaction; | A n/a B n/a C 62% |
A
1,3-di-tert-butylurea
B
3-methyl-N-(pyridin-2-yl)benzamide
C
tert-butylamine
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Schlenk technique; Heating; chemoselective reaction; | A n/a B 61% C n/a |
N-tert-butyl-2-p-tolyl-1H-imidazo[1,2-a]pyridine-3-amine
A
1,3-di-tert-butylurea
B
4-methyl-N-(pyridine-2-yl)benzamide
C
tert-butylamine
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Schlenk technique; Heating; chemoselective reaction; | A n/a B 60% C n/a |
N-tert-butyl-2-(3-methoxyphenyl)imidazo[1,2-a]pyridin-3-amine
A
1,3-di-tert-butylurea
B
2-methoxy-N-(pyridin-2-yl)benzamide
C
tert-butylamine
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Schlenk technique; Heating; chemoselective reaction; | A n/a B 59% C n/a |
A
5-methyl-N-(pyridin-2-yl)furan-2-carboxamide
B
1,3-di-tert-butylurea
C
tert-butylamine
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Schlenk technique; Heating; chemoselective reaction; | A 59% B n/a C n/a |
N-(tert-butyl)-2-(2-chlorophenyl)imidazo[1,2-a]pyridin-3-amine
A
1,3-di-tert-butylurea
B
2-chloro-N-(pyridine-2-yl)benzamide
C
tert-butylamine
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Schlenk technique; Heating; chemoselective reaction; | A n/a B 58% C n/a |
A
N-(pyridine-2-yl)propionamide
B
1,3-di-tert-butylurea
C
tert-butylamine
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Schlenk technique; Heating; chemoselective reaction; | A 57% B n/a C n/a |
N-tert-butyl-2-(3-nitrophenyl)imidazo[1,2-a]pyridin-3-amine
A
1,3-di-tert-butylurea
B
tert-butylamine
C
3-nitro-N-(pyridin-2-yl)benzamide
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Schlenk technique; Heating; chemoselective reaction; | A n/a B n/a C 56% |
N-(3-phenylprop-2-yn-1-ylidene)-t-butylamine
2-mercapto-4(5)-phenylimidazole
B
tert-butylamine
Conditions | Yield |
---|---|
Stage #1: N-(3-phenylprop-2-yn-1-ylidene)-t-butylamine; 2-mercapto-4(5)-phenylimidazole In methanol at 60℃; for 0.5h; Stage #2: With water In methanol | A 50% B n/a |
(E)-3-Phenyl-acrylic acid 1-tert-butylcarbamoyl-1-methyl-2-oxo-propyl ester
A
N-tert.butyl 2-acetyl 2-hydroxy propanamide
B
tert-butylamine
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; cesium fluoride In tetrahydrofuran for 72h; Heating; | A 45% B n/a |
Conditions | Yield |
---|---|
With ammonia; zeolite BEA (Si/Al ratio of 12.5) at 250℃; under 22502.3 Torr; Product distribution / selectivity; | 44.78% |
With ammonia; MF114 zeolite at 274.9℃; under 30002.4 Torr; | 8.9% |
With ammonia; sodium at 250℃; under 661957 Torr; |
Conditions | Yield |
---|---|
Stage #1: N-tert-butylbenzylamine With rhodium(III) tetra(p-sulfonato-phenyl)porphyrin; oxygen; benzaldehyde In methanol; water at 100℃; under 750.075 Torr; for 6h; Stage #2: With hydrogenchloride In methanol; water at 80℃; Catalytic behavior; | 24.5% |
Conditions | Yield |
---|---|
Stage #1: N-isopropyl-N-tert-butylamine With rhodium(III) tetra(p-sulfonato-phenyl)porphyrin; oxygen; benzaldehyde In methanol; water at 100℃; under 750.075 Torr; for 6h; Stage #2: With hydrogenchloride In methanol; water at 80℃; Catalytic behavior; | 22% |
Bis-tert.-butylamino-phenylboran
A
(t-butylimino)phenylborane
B
tert-butylamine
Conditions | Yield |
---|---|
A n/a B 12% | |
A n/a B 12% |
Conditions | Yield |
---|---|
In dichloromethane for 18h; Molecular sieve; | 100% |
at 20℃; for 2h; | 100% |
In dichloromethane at 20℃; for 4h; | 100% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; Na12[WZn3(H2O)2(ZnW9O34)2] at 75℃; for 7h; | 100% |
With potassium permanganate In water 1.) 11 deg C -> room temperature, 8 h, 2.) 55 deg C, 18 h; | 78% |
With sodium permanganate In hexane at 69℃; for 24h; | 76% |
maleic anhydride
tert-butylamine
(Z)-4-(tert-butylamino)-4-oxo-2-butenoic acid
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 2h; | 100% |
In toluene at 45 - 50℃; for 1h; | 94% |
In diethyl ether at 20℃; | 89% |
succinic acid anhydride
tert-butylamine
4-(tert-butylamino)-4-oxobutanoic acid
Conditions | Yield |
---|---|
Stage #1: succinic acid anhydride; tert-butylamine In N,N-dimethyl acetamide at 20℃; for 24h; Stage #2: In N,N-dimethyl acetamide; xylene at 140℃; for 48h; | 100% |
In dichloromethane at 20℃; for 1h; | 52% |
Stage #1: succinic acid anhydride; tert-butylamine In dichloromethane at 20℃; for 1h; Stage #2: With sodium hydroxide In water at 20℃; for 2h; Stage #3: With hydrogenchloride In water at 0℃; | 52% |
4-methoxy-benzoyl chloride
tert-butylamine
N-tert-butyl-4-methoxybenzamide
Conditions | Yield |
---|---|
With sodium hydroxide In dichloromethane | 100% |
With dmap; sodium hydroxide In dichloromethane at 0 - 20℃; | 100% |
In tetrahydrofuran at 0℃; | 86% |
ethyl 5-oxo-2-phenyl-2,5-dihydroisoxazole-4-carboxaldehyde
tert-butylamine
ethyl (N-t-butylcarbamoyl)(N-phenylcarbamoyl)acetate
Conditions | Yield |
---|---|
In acetone at 25℃; | 100% |
Conditions | Yield |
---|---|
In chloroform at 0℃; | 100% |
With hydrogenchloride In dichloromethane at 0 - 20℃; for 0.666667h; | 97% |
With triethylamine In dichloromethane at 20℃; | 95% |
Phenyl glycidyl ether
tert-butylamine
1-(N-tert-butyl)amino-3-phenoxy-2-propanol
Conditions | Yield |
---|---|
In 2,2,2-trifluoroethanol at 20℃; for 6h; regioselective reaction; | 100% |
With lithium perchlorate In diethyl ether at 20℃; for 0.5h; | 96% |
In water at 0 - 20℃; | 96% |
2,4-Dinitrofluorobenzene
tert-butylamine
N-tert-butyl-2,4-dinitro-aniline
Conditions | Yield |
---|---|
With 2-hydroxypyridin In benzene at 25℃; Rate constant; other catalysts, other solvents, var. conc. of catalysts; | 100% |
4-bromo-benzaldehyde
tert-butylamine
N-(4-bromobenzylidene)-2-methylpropan-2-amine
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 4h; | 100% |
With 4 A molecular sieve for 24h; Ambient temperature; | 97% |
With titanium tetrachloride In diethyl ether; toluene at 0℃; for 0.25h; Glovebox; Inert atmosphere; Schlenk technique; | 86% |
at 100℃; Schlenk technique; | |
In 1,2-dichloro-ethane at 70℃; for 4h; Glovebox; |
formaldehyd
2,2,5,5-tetramethyl-4-nitromethyleneimidazolidine-1-oxyl
tert-butylamine
Conditions | Yield |
---|---|
In methanol; water | 100% |
2-chloroacetylenephosphonic acid dimethyl ester
tert-butylamine
dimethyl <2-(tert-butylimino)vinyl>phosphonate
Conditions | Yield |
---|---|
100% | |
In diethyl ether for 2h; Ambient temperature; | 98% |
In diethyl ether at -10 - 20℃; | 98% |
In diethyl ether at -5 - 20℃; for 2h; | 98% |
bis(3-(trifluoromethyl)benzenesulfonyl) peroxide
tert-butylamine
A
N-t-Butyl-O-m-trifluoromethylbenzenesulfonylhydroxylamine
Conditions | Yield |
---|---|
In diethyl ether at -78℃; for 2h; | A 90% B 100% |
6-methylhepto-5-enal
tert-butylamine
6-methylhept-5-en-1-al tert-butylimine
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 1.5h; | 100% |
Conditions | Yield |
---|---|
In diethyl ether at -78℃; for 2h; | A 87% B 100% |
(2-formylphenyl)(diphenyl)phosphine
tert-butylamine
N-(tert-butyl)-2-[(diphenylphosphino)benzylidene]amine
Conditions | Yield |
---|---|
In methanol; dichloromethane at 20℃; for 2h; Inert atmosphere; | 100% |
In toluene at 150 - 160℃; for 6h; Inert atmosphere; | 96% |
With molecular sieve for 2h; Heating; | 93% |
In toluene at 110℃; for 18h; Inert atmosphere; Molecular sieve; Sealed tube; Schlenk technique; | 73% |
Heating; |
1-(phenylsulfonyl)indole-3-carbaldehyde
tert-butylamine
3-((tert-butylimino)methyl)-1-(phenylsulfonyl)indole
Conditions | Yield |
---|---|
In benzene for 24h; Heating; | 100% |
In benzene 1.) RT, 1 h, 2.) reflux, 2 h; |
N-<2,4,6-tri(tert-butyl)phenyl>phosphenimidous acid 2,6-di-tert-butyl-4-methylphenyl ester
tert-butylamine
Conditions | Yield |
---|---|
In benzene for 240h; | 100% |
In diethyl ether at 20℃; | 100 % Spectr. |
(2-formylphenyl)butyl tellurium dibromide
tert-butylamine
2-(tert-butyliminomethinyl)phenyltellurenyl bromide
Conditions | Yield |
---|---|
With trifluoroacetic acid In benzene | 100% |
(Z)-6,10-Dimethyl-5,9-undecadienal
tert-butylamine
(Z)-6,10-Dimethyl-5,9-undecadienal tert-butylimine
Conditions | Yield |
---|---|
In diethyl ether 1.) -10 deg C, 30 min, 2.) room temp., 1.5 h; | 100% |
In diethyl ether at 20℃; for 1.5h; |
Conditions | Yield |
---|---|
100% |
1,2,2,5,5,6,6-heptamethyl-3-methylene-4-piperidone
tert-butylamine
1,2,2,3,3,6,6-heptamethyl-5-tert-butylaminomethyl-4-piperidone
Conditions | Yield |
---|---|
In ethanol at 25℃; for 168h; | 100% |
N-(bis-p-methoxyphenylphosphinoyl)-O-methylsulphonylhydroxylamine
tert-butylamine
N',P-bis-p-methoxyphenyl-N-t-butylphosphonic diamide
Conditions | Yield |
---|---|
100% |
tert-butylamine
p-methoxybenzyl chloride
N-(p-methoxybenzyl)-N-tert-butylamine
Conditions | Yield |
---|---|
100% | |
With sodium carbonate; sodium iodide In N,N-dimethyl-formamide at 65℃; for 4h; Inert atmosphere; | 56% |
In N,N-dimethyl-formamide for 6h; Yield given; |
tert-butylamine
bis(hydroxymethyl)phenylphosphine
1,5-Di(tert-butyl)-3,7-diphenyl-1,5-diaza-3,7-diphosphacyclooctane
Conditions | Yield |
---|---|
In ethanol | 100% |
tert-butylamine
3,5-di-t-butyl-4-hydroxybenzaldehyde
4-<(N-tert-butylimino)methyl>-2,6-di-tert-butylphenyl
Conditions | Yield |
---|---|
In ethanol for 3h; Heating; | 100% |
tert-butylamine
1,1-dichloro-5-aza-2,8-dioxa-1-phosphaV-dibenzo<9,9',11,11'-tetra-tert-butyl>-bicyclo<3.3.0>octadiene
Conditions | Yield |
---|---|
In benzene for 2h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
In ethanol at 20℃; Cooling with ice; | 81% |
tert-butylamine
N,N-dimethyl-5,7-bis(trifluoroacetyl)-8-quinolylamine
Conditions | Yield |
---|---|
In acetonitrile at 50℃; for 72h; | 100% |
In acetonitrile at 50℃; for 72h; Substitution; | 100% |
Conditions | Yield |
---|---|
aluminum oxide; zinc(II) oxide at 100℃; for 2h; Condensation; | 100% |
In water at 20℃; for 1h; Green chemistry; | 93% |
In water at 20℃; for 1h; Green chemistry; | 93% |
Stage #1: carbon disulfide; tert-butylamine In water at 35℃; for 1h; Large scale; Stage #2: With dihydrogen peroxide In vaseline at 65℃; for 2h; Temperature; Large scale; |
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