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Benzenecarboximidic acid, 4-methoxy-, methyl ester, hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39739-49-6

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39739-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39739-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,3 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39739-49:
(7*3)+(6*9)+(5*7)+(4*3)+(3*9)+(2*4)+(1*9)=166
166 % 10 = 6
So 39739-49-6 is a valid CAS Registry Number.

39739-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-methoxybenzimidate hydrochloride

1.2 Other means of identification

Product number -
Other names 4-methoxy-benzimidic acid methyl ester, hydrochloride

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:39739-49-6 SDS

39739-49-6Relevant academic research and scientific papers

Transition-metal-free approach to 4-ethynylpyrimidines via alkenynones

Golubev, Pavel R.,Pankova, Alena S.,Kuznetsov, Mikhail A.

, p. 3614 - 3621 (2014/06/23)

A practical approach to the synthesis of 4-ethynylpyrimidines by the condensation of arylamidines with 2-aryl-1-ethoxy-5-(trimethylsilyl)pent-1-en-4- yn-3-ones has been developed. As these latter ketones are easily accessible from bis(trimethylsilyl)acetylene and arylacetyl chlorides, the regioselective condensation reported herein provides a facile access to both TMS-protected and unprotected 4-ethynylpyrimidines in yields of up to 85%. Copyright

Efficient synthesis of α-tertiary α-silylamines from aryl sulfonylimidates via one-pot, sequential C-Si/C-C bond formations

Han, Xiao-Jun,Yao, Ming,Lu, Chong-Dao

supporting information; experimental part, p. 2906 - 2909 (2012/07/14)

An efficient and flexible route for the synthesis of α-tertiary (α,α-dibranched) α-silylamines via sequential reactions of sulfonylimidates using readily available phenyldimethylsilyllithium and Grignard reagents is described. The procedure allows successive formation of C-Si/C-C bonds in a single flask.

6-1H-IMIDAZO-QUINAZOLINE AND QUINOLINES DERIVATIVES, NEW MAO INHIBITORS AND IMIDAZOLINE RECEPTOR LIGANDS

-

Page/Page column 35, (2010/01/12)

The present invention is directed to 6-(1H-imidazo-1-yl)-2-aryl and 2-heteroaryl quinazoline and quinolines derivatives, compounds of formula (I), their pharmaceutical acceptable salts and solvates and corresponding pharmaceutical compositions, that acts

Pyrimidine derivatives and drugs

-

, (2008/06/13)

The object of the present invention is to obtain new class of compounds which have improving effect on learning and memory disorders with good selectivity in central nervous system and little side effects and then to provide a good medicine for treatment

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