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70288-74-3

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70288-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70288-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,8 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70288-74:
(7*7)+(6*0)+(5*2)+(4*8)+(3*8)+(2*7)+(1*4)=133
133 % 10 = 3
So 70288-74-3 is a valid CAS Registry Number.

70288-74-3SDS

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 (2S)-2-(methoxycarbonylamino)propanoate

1.2 Other means of identification

Product number -
Other names N-(METHOXYCARBONYL)-ALANINE METHYL ESTER

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:70288-74-3 SDS

70288-74-3Downstream Products

70288-74-3Relevant articles and documents

DIAZAPHOSPHACYCLES

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Page/Page column 80, (2008/06/13)

Diazaphosphacycles comprising compounds having the formula XI : and salts of the compound are provided, wherein the variables W, T, R1, R14, and R15 are as described herein. Transition metal catalysts incorporating such diazaphosphacycles and methods of u

Process for the production of aminoacid hydrochlorides/or diaminoacid dihydrochlorides

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, (2008/06/13)

Aminoacid hydrochlorides or diaminoacid dihydrochlorides are produced by first reacting a halocarboxylic acid ester with an alkali metal cyanate in the presence of an alcohol to form the corresponding mono- or diurethane and then saponifying this to the corresponding mono- or dihydrochloride. The new process is relatively versatile in its use and above all opens up an elegant synthesis route for lysine.

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