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194278-12-1

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194278-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194278-12-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,2,7 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 194278-12:
(8*1)+(7*9)+(6*4)+(5*2)+(4*7)+(3*8)+(2*1)+(1*2)=161
161 % 10 = 1
So 194278-12-1 is a valid CAS Registry Number.

194278-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-[(2-ethoxy-2-oxoethyl)amino]benzoate

1.2 Other means of identification

Product number -
Other names methyl 2-((2-ethoxy-2-oxoethyl)amino)benzoate

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:194278-12-1 SDS

194278-12-1Relevant articles and documents

Novel 1,3- spirocyclization reaction in the photochemistry of anthranilic acid derivatives in acetonitrile

Sharshira, Essam Mohamed

, p. 527 - 534 (2007/10/03)

Anthranilic acid derivatives 1a-c were irradiated in acetonitrile solution to give imines (rearranged products) 2a-c in each case. In the case of 1c, a diastereomeric mixture of dl- and meso-dibenzoate derivative (dimerization product) 3c was also obtaine

Regiospecific functionalization of indole-2-carboxylates and diastereoselective preparation of the corresponding indolines

Collot, Valerie,Schmitt, Martine,Marwah, Padma,Bourguignon, Jean-Jacques

, p. 2823 - 2847 (2007/10/03)

The N-acyl derivatives of 3-substituted indole-2-carboxylates prepared through several routes were submitted to catalytic hydrogenation affording either cis- or trans-indoline diastereomers after quantitative C-2 epimerization.

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