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dimethyl 1-(1-oxo-1-phenylpropan-2-yl)hydrazine-1,2-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86358-61-4

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86358-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86358-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,5 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86358-61:
(7*8)+(6*6)+(5*3)+(4*5)+(3*8)+(2*6)+(1*1)=164
164 % 10 = 4
So 86358-61-4 is a valid CAS Registry Number.

86358-61-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 1-(1-oxo-1-phenylpropan-2-yl)hydrazine-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:86358-61-4 SDS

86358-61-4Downstream Products

86358-61-4Relevant academic research and scientific papers

Frustrated Lewis acid/Br?nsted base catalysts for direct enantioselective α-amination of carbonyl compounds

Shang, Ming,Wang, Xiaoxu,Koo, Seung Moh,Youn, Jennifer,Chan, Jessica Z.,Yao, Wenzhi,Hastings, Brian T.,Wasa, Masayuki

supporting information, p. 95 - 98 (2017/05/16)

A method for enantioselective direct α-amination reaction catalyzed by a sterically "frustrated" Lewis acid/Br?nsted base complex is disclosed. Cooperative functioning of the Lewis acid and Br?nsted base components gives rise to in situ enolate generation from monocarbonyl compounds. Subsequent reaction with hydrogen-bond activated dialkyl azodicarboxylates delivers α-aminocarbonyl compounds in high enantiomeric purity.

SYNTHESIS OF α-DIALKYLAMINOSTYRENES AND THEIR REACTION WITH AZODICARBOXYLIC ESTER AND COMPOUNDS CONTAINING AN ACTIVATED MULTIPLE BOND

Koikov, L. N.,Terent'ev, P. B.,Torochesnikov, V. N.,Kulikov, N. S.

, p. 110 - 118 (2007/10/02)

Lower α-dialkylaminostyrenes react with compounds containing an activated double bond by a mechanism of "vinyl" substitution with the formation of both disubstituted and monosubstituted compounds.The ester groups of the mono- and bisN,N'-di(methoxycarbon

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