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Cas:99-07-0
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inquiryThe 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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Cas:99-07-0
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inquiryAs a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem’s R&D center offer custom synthesis according to the contract research and development services for t
Cas:99-07-0
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inquiryOur 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
Cas:99-07-0
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inquiry99-07-0 3-Dimethylaminophenol Now we would like to update our product list for you, kindly check the below information: 1. Catalyst series ( such as Noble Metal Catalyst, Phosphorous ligand, etc ) 2. Pharmaceutical Intermediate (
Cas:99-07-0
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inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:99-07-0
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inquiryProduct Description Product Name 3-Dimethylaminophenol CAS No. 99-07-0 Appearance White powder
Cas:99-07-0
Min.Order:1 Gram
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inquiryAppearance:violet powder Storage:room temperature Package:25kg/drum Application:3-Dimethylaminophenol can be used as neostigmine bromide intermediate and dye intermediate. Transportation:Express/Sea/Air Port:any port in china
Cas:99-07-0
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inquiry1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
Cas:99-07-0
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inquiry3-Dimethylaminophenol Basic information Product Name: 3-Dimethylaminophenol Synonyms: N N DIMETHYL-M-AMINOPHENOL;N,N-DIMETHYL-M-HYDROXYANILINE;N,N-DIMETHYL-3-AMINOPHENOL;(3-Hydroxyphenyl)dimethylamine;3-(dimethylamino)-pheno;JACS-99-07-0;3-(Dim
Cas:99-07-0
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inquiryOur 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 prese
Cas:99-07-0
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inquiry3-Dimethylaminophenol CAS:99-07-0 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic interm
Cas:99-07-0
Min.Order:1 Gram
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
Cas:99-07-0
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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
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Hangzhou 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:99-07-0
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inquiryCompany Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
Cas:99-07-0
Min.Order:1 Gram
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Type:Lab/Research institutions
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
best quality 99-07-0 top purity 3-Dimethylaminophenol Molecular Formula (CH3)2NC6H4OH Molar Mass 137.18 Density 1.089g/cm3 Melting Point 80-85℃ Boling Point 266.5°C at 760 mmHg
Cas:99-07-0
Min.Order:1 Gram
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Type:Other
inquiryMassive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
Cas:99-07-0
Min.Order:1 Gram
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inquiryZibo 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:99-07-0
Min.Order:10 Gram
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inquiryWe are one of a few suppliers that can offer custom synthesis service of this product We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are committed to prov
Cas:99-07-0
Min.Order:100 Gram
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inquirySuperior quality, moderate price & quick delivery. Appearance:brown powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag,or as your request Application:Used as Pharmaceutical Intermediates Transporta
Established in May 2015, TaiChem Ltd. is initially invested by a British research and development company and started by PhDs back from aboard. The company is registered in China Medical City (CMC), Taizhou, Jiangsu Province, and the production site
Cas:99-07-0
Min.Order:10 Gram
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Type:Lab/Research institutions
inquiryProduct name: 3-Dimethylaminophenol CAS No.:99-07-0 Molecule Formula:C8H11NO Molecule Weight:137.18 Purity: 99.0% Package: 25kg/bag Description:Light grey to white crystalline powder Manufacture Standards:Enterprise Standard
Cas:99-07-0
Min.Order:1 Kilogram
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Type:Trading Company
inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
Cas:99-07-0
Min.Order:1 Gram
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inquiryOur Advantages A. International Top level TechnologyOur company owned biomedicine experts are famous at home and abroad with rich experience in research and development in the field of efficient chiral functional molecules research and development an
3-methoxy-N,N-dimethylaniline
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With boron trichloride; tetra-(n-butyl)ammonium iodide In dichloromethane at -78 - 0℃; for 1h; dealkylation; | 95% |
Conditions | Yield |
---|---|
With hydrogen In water at 200℃; under 375.038 Torr; for 3h; Reagent/catalyst; Autoclave; | 93% |
Conditions | Yield |
---|---|
With copper(l) iodide; 6,7-dihydro-5H-quinolin-8-one oxime; potassium hydroxide In water at 25℃; for 24h; Inert atmosphere; | 91% |
methanesulfonic acid 3-dimethylaminophenyl ester
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With lithium diisopropyl amide In tetrahydrofuran at 0℃; for 0.0166667h; | 89% |
Conditions | Yield |
---|---|
With copper(l) iodide; 6,7-dihydro-5H-quinolin-8-one oxime; potassium hydroxide In water at 85℃; for 24h; Inert atmosphere; | 89% |
3-Dimethylaminophenol
Conditions | Yield |
---|---|
In water-d2 for 0.5h; Inert atmosphere; Photolysis; | 89% |
N,N-dimethyl-aniline
A
4-(N,N-dimethylamino)phenol
B
2-hydroxy-N,N-dimethylaniline
C
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With dihydrogen peroxide; antimony pentafluoride In hydrogen fluoride at -20℃; for 0.25h; Mechanism; Product distribution; | A 26% B 14% C 44% |
With hydrogen fluoride; dihydrogen peroxide; antimony pentafluoride at -20℃; for 0.25h; | A 26% B 14% C 44% |
With dihydrogen peroxide; antimony pentafluoride In hydrogen fluoride at -20℃; for 0.25h; | A 26% B 14% C 44% |
Conditions | Yield |
---|---|
With hydrogen In methanol at 180℃; under 12751.3 Torr; for 8h; Autoclave; | 21% |
With sodium tetrahydroborate In methanol at 20℃; |
Conditions | Yield |
---|---|
at 170℃; |
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
bei der Natronschmelze; | |
bei der Natronschmelze; |
Conditions | Yield |
---|---|
bei der Destillation unter vermindertem Druck; |
4-Aminosalicylic acid
dimethyl sulfate
A
4-dimethylamino-2-hydroxy-benzoic acid methyl ester
B
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
With sulfuric acid at 55 - 60℃; und Behandeln mit Natron bei 270-300grad; | |
Multi-step reaction with 2 steps 1: sulfuric acid 2: bei der Natronschmelze View Scheme |
N,N-dimethylammonium chloride
dimethyl amine
recorcinol
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With water at 200℃; |
carbonic acid bis-(3-dimethylamino-phenyl ester)
aniline
A
N,N-diphenylurea
B
3-Dimethylaminophenol
Conditions | Yield |
---|---|
at 190℃; |
Conditions | Yield |
---|---|
ueber die Diazonium-Verbindung; | |
With sulfuric acid Diazotization.und Kochen der Diazoniumsalzloesung; |
2-amino-4-hydroxy-benzenesulfonic acid
methyl iodide
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With potassium hydroxide; water at 100 - 110℃; und Behandeln des Reaktionsprodukts mit methylschfefelsaurem Natrium in waessr. Loesung im Autoklaven auf 170-180grad; |
Neostigmine bromide
A
Dimethylcarbaminsaeure-3-aminophenylester
B
norneostigmine
C
Dimethylcarbaminsaeure-3-methylaminophenylester
D
3-hydroxyphenyltrimethylammonium bromide
E
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With water In various solvent(s) at 70 - 95℃; Kinetics; Thermodynamic data; Product distribution; Activation energies in 6 buffer systems with varying pH, influence of buffer concentration, ionic force, oxygen, and pilocarpine hydrochloride on the rates of hydrolysis and demethylation; |
ethyl [7-(dimethylamino)-2-oxo-2H-chromen-4-yl]acetate
3-Dimethylaminophenol
Conditions | Yield |
---|---|
at 170℃; |
Conditions | Yield |
---|---|
With water at 125℃; |
3-Dimethylaminophenol
Conditions | Yield |
---|---|
durch Destillation unter vermindertem Druck; |
sulfuric acid
3-(dimethylamino)phenyl carbonochloridate
A
hydrogenchloride
B
carbon dioxide
C
3-Dimethylaminophenol
hydrogenchloride
N,N,N',N'-tetramethyl-m-phenylenediamine
A
3-Dimethylaminophenol
B
recorcinol
Conditions | Yield |
---|---|
at 180℃; |
Neostigmine bromide
A
Dimethylcarbaminsaeure-3-aminophenylester
B
norneostigmine
C
Dimethylcarbaminsaeure-3-methylaminophenylester
D
3-hydroxyphenyltrimethylammonium bromide
E
3-Dimethylaminophenol
Conditions | Yield |
---|---|
Heating; degradation in alkaline solution; |
methyl yellow
A
4-amino-phenol
B
N,N-dimethyl-aniline
C
aniline
D
N,N-Dimethyl-4-nitroaniline
E
3-Dimethylaminophenol
F
recorcinol
G
phenol
Conditions | Yield |
---|---|
With ferrous(II) sulfate heptahydrate; sulfuric acid; water; dihydrogen peroxide at 25℃; pH=1.8; Kinetics; |
N,N-dimethyl-formamide
3-Dimethylaminophenol
4-dimethylamino-2-hydroxy-benzaldehyde
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-formamide With trichlorophosphate for 0.0833333h; Stage #2: 3-Dimethylaminophenol at 20 - 70℃; for 2h; | 100% |
With methanesulfonyl chloride at 20 - 100℃; for 1h; | 90.9% |
Stage #1: N,N-dimethyl-formamide With trichlorophosphate at 20℃; Inert atmosphere; Stage #2: 3-Dimethylaminophenol at 20 - 90℃; Vilsmeier-Haack reaction; Inert atmosphere; Stage #3: With water | 70% |
Conditions | Yield |
---|---|
With silver trifluoromethanesulfonate at 60℃; for 0.05h; neat (no solvent); | 99% |
und man destilliert das Produkt im Vakuum; |
Conditions | Yield |
---|---|
With triethylamine | 99% |
benzyl bromide
3-Dimethylaminophenol
N-benzyl-3-hydroxy-N,N-dimethylanilinium bromide
Conditions | Yield |
---|---|
In acetonitrile | 98% |
In acetonitrile at 20℃; |
4-nitrobenzaldehdye
3-Dimethylaminophenol
6,6’-((4-nitrophenyl)methylene)bis(3-(dimethylamino)phenol)
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid; acetic acid at 60℃; for 14h; Inert atmosphere; | 98% |
C17H13F3N2O2
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With C37H34N4O3 In chloroform at 20℃; for 8h; Inert atmosphere; enantioselective reaction; | 98% |
Conditions | Yield |
---|---|
With [Ru(κ1-OAc)(κ2-OAc)(κ3-1,1,1-tris(diphenylphosphinomethyl)ethane)] In acetonitrile at 70℃; for 1h; Inert atmosphere; Schlenk technique; | 98% |
3-Dimethylaminophenol
(2-formyl-11-methoxycarbonylmethyl-14-methyl-6,7,10,11,17,18-hexahydro-9H-8,16,19-trioxa-5,11-diaza-dibenzo[a,g]cyclopentadecen-5-yl)-acetic acid methyl ester
[2-(3,6-bis-dimethylamino-9H-xanthen-9-yl)-11-methoxycarbonylmethyl-14-methyl-6,7,10,11,17,18-hexahydro-9H-8,16,19-trioxa-5,11-diaza-dibenzo[a,g]cyclopentadecen-5-yl]-acetic acid methyl ester
Conditions | Yield |
---|---|
toluene-4-sulfonic acid In propionic acid at 60℃; | 97% |
With toluene-4-sulfonic acid; propionic acid |
Conditions | Yield |
---|---|
toluene-4-sulfonic acid In propionic acid at 60℃; for 16h; | 97% |
Conditions | Yield |
---|---|
With acetic acid at 20℃; | A 97% B n/a |
Conditions | Yield |
---|---|
With 5% Rh/C; oxygen; trifluoroacetic acid at 60℃; for 34h; | 97% |
triisopropylsilyl trifluoromethanesulfonate
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 22h; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
Stage #1: 3-Dimethylaminophenol With potassium hydroxide In toluene at 90℃; for 1h; Reflux; Stage #2: 4-nitrophenyl dimethylcarbamate In toluene for 3h; Product distribution / selectivity; Reflux; | 96.2% |
malonic acid bis-(2,4,6-trichloro-phenyl) ester
3-Dimethylaminophenol
7-(dimethylamino)-4-hydroxy-2H-1-benzopyran-2-one
Conditions | Yield |
---|---|
In toluene at 110℃; for 4h; | 96% |
Conditions | Yield |
---|---|
With 1-(4-ferrocenylbutyl)-3-{3-[dihydroxy(methoxy)silyl]propyl}benzimidazol-3-ium chloride supported on Fe3O4(at)SiO2 core-shell/BiOCl nano-composite In ethanol; water at 20℃; for 0.333333h; Sonication; | 95% |
Stage #1: 4-nitrobenzaldehdye; malononitrile With polyethyleneimine covalently bound on the surface of Fe3O4 magnetic nanoparticle by [3-(2,3-epoxypropoxy)propyl]trimethoxysilane as cross linker In water for 0.0166667h; Sonication; Green chemistry; Stage #2: 3-Dimethylaminophenol In water for 1.5h; Reagent/catalyst; Time; Temperature; Sonication; Green chemistry; | 94% |
With mesoporous Al-MCM-41 functionalized by layered double hydroxide nanosheets and (3-aminopropyl)triethoxysilane In ethanol at 80℃; for 6h; Schlenk technique; | 91% |
3-Dimethylaminophenol
6-chloro-1-[(4-methoxyphenyl)methyl]-4-(trifluoromethyl)hydroquinazolin-2-one
Conditions | Yield |
---|---|
With C37H34N4O3 In chloroform at 20℃; for 2h; Inert atmosphere; enantioselective reaction; | 95% |
N,N-diethylcarbamyl chloride
3-Dimethylaminophenol
3-<<(diethylamino)carbonyl>oxy>-N,N-dimethylaniline
Conditions | Yield |
---|---|
With pyridine; triethylamine In tetrahydrofuran Reflux; Inert atmosphere; | 94% |
With sodium hydride 1.) diethyl ether, DMF, 15 min, 2.) RT, 1.5 h; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With 6A-{{2-{{2-[(2-aminoethyl)amino]ethyl}amino}ethyl}amino}-6A-deoxy-β-cyclodextrin In water at 20℃; for 6h; chemoselective reaction; | 94% |
With 2-amino-2-hydroxymethyl-1,3-propanediol In ethanol; water at 20℃; for 3.5h; Green chemistry; | 83% |
With piperidine In ethanol at 20℃; | 31% |
4-chlorobenzaldehyde
malononitrile
3-Dimethylaminophenol
2-amino-4-(4-chlorophenyl)-7-dimethylamino-4H-chromene-3-carbonitrile
Conditions | Yield |
---|---|
With 1-(4-ferrocenylbutyl)-3-{3-[dihydroxy(methoxy)silyl]propyl}benzimidazol-3-ium chloride supported on Fe3O4(at)SiO2 core-shell/BiOCl nano-composite In ethanol; water at 20℃; for 0.333333h; Sonication; | 94% |
With mesoporous Al-MCM-41 functionalized by layered double hydroxide nanosheets and (3-aminopropyl)triethoxysilane In ethanol at 80℃; for 6h; Schlenk technique; | 90% |
With 2-amino-2-hydroxymethyl-1,3-propanediol In ethanol; water at 20℃; for 2.5h; Green chemistry; | 85% |
With piperidine In ethanol at 35℃; for 12h; |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 0 - 20℃; | 94% |
With potassium carbonate; potassium iodide In acetone Reflux; | 81% |
With potassium carbonate In acetonitrile at 0 - 20℃; | 43% |
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 20℃; for 8h; Nosylation; | 93% |
diethyl cyanophosphonate
3-Dimethylaminophenol
phosphoric acid diethyl ester-(3-dimethylamino-phenyl ester)
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; for 0.5h; phosphorylation; | 93% |
Conditions | Yield |
---|---|
With piperidine In ethanol at 20℃; | 93% |
With 1-(4-ferrocenylbutyl)-3-{3-[dihydroxy(methoxy)silyl]propyl}benzimidazol-3-ium chloride supported on Fe3O4(at)SiO2 core-shell/BiOCl nano-composite In ethanol; water at 20℃; for 0.466667h; Sonication; | 85% |
With 2-amino-2-hydroxymethyl-1,3-propanediol In ethanol; water at 20℃; for 3h; Green chemistry; | 84% |
3-Dimethylaminophenol
2-(11-carbamoylmethyl-2-formyl-14-methyl-6,7,10,11,17,18-hexahydro-9H-8,16,19-trioxa-5,11-diaza-dibenzo[a,g]cyclopentadecen-5-yl)-acetamide
Conditions | Yield |
---|---|
toluene-4-sulfonic acid In propionic acid at 60℃; | 93% |
3-nitro-benzaldehyde
malononitrile
3-Dimethylaminophenol
2-amino-7-(dimethylamino)-4-(3-nitrophenyl)-4H-chromene-3-carbonitrile
Conditions | Yield |
---|---|
Stage #1: 3-nitro-benzaldehyde; malononitrile With polyethyleneimine covalently bound on the surface of Fe3O4 magnetic nanoparticle by [3-(2,3-epoxypropoxy)propyl]trimethoxysilane as cross linker In water for 0.0166667h; Sonication; Green chemistry; Stage #2: 3-Dimethylaminophenol In water for 1.5h; Sonication; Green chemistry; | 93% |
With 1-(4-ferrocenylbutyl)-3-{3-[dihydroxy(methoxy)silyl]propyl}benzimidazol-3-ium chloride supported on Fe3O4(at)SiO2 core-shell/BiOCl nano-composite In ethanol; water at 20℃; for 0.366667h; Sonication; | 90% |
With mesoporous Al-MCM-41 functionalized by layered double hydroxide nanosheets and (3-aminopropyl)triethoxysilane In ethanol at 80℃; for 6h; Schlenk technique; | 89% |
With 2-amino-2-hydroxymethyl-1,3-propanediol In ethanol; water at 20℃; for 2h; Green chemistry; | 87% |
With piperidine In ethanol at 35℃; for 12h; |
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With C37H34N4O3 In chloroform at 20℃; for 3.5h; Inert atmosphere; enantioselective reaction; | 93% |
Conditions | Yield |
---|---|
With Difluoroacetic acid; 5% palladium on Al2O3; oxygen at 20℃; for 18h; | 93% |
4,5-dichlorophthalonitrile
3-Dimethylaminophenol
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 18h; Inert atmosphere; | 93% |
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 18h; | 93% |
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