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13157-96-5

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13157-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13157-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13157-96:
(7*1)+(6*3)+(5*1)+(4*5)+(3*7)+(2*9)+(1*6)=95
95 % 10 = 5
So 13157-96-5 is a valid CAS Registry Number.

13157-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl chloro(methoxy)acetate

1.2 Other means of identification

Product number -
Other names 2-chloro-2-methoxy-acetic acid 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:13157-96-5 SDS

13157-96-5Relevant articles and documents

Total synthesis of the proposed structure of briarellin J

Crimmins, Michael T.,Mans, Mark C.,Rodriguez, Abimael D.

, p. 5028 - 5031 (2010)

The total synthesis of the originally proposed structure of briarellin J is reported in 15 steps from a known compound and in 23 steps from readily available materials. Key reactions include an exo-selective intramolecular Diels-Alder and a substrate-cont

Benzannelated derivatives, their manufacture and use as pharmaceutical agents

-

Page/Page column 24, (2008/06/13)

There are presented compounds of the formula wherein R6 and R7 is R4 and R5 or R5 and R6 together with the carbon atoms to which they are attached, form a ring as defined in the description

Cephem derivatives

-

, (2008/06/13)

What are disclosed are cephem compounds of the formula STR1 in which R1 denotes hydrogen, an optionally substituted alkyl, acyl, arylsulfonyl or alkylsulfonyl group or an amino-protective group which is known from peptide chemistry, R2 denotes hydrogen or an optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, aralkyl, acyl, aryl, arylsulfonyl, alkylsulfonyl or heterocyclic group, R3 denotes hydrogen, an ester group or a cation, R4 denotes hydrogen, a lower alkoxy group or a group which can be converted to this, X denotes a SO group in the R or S configuration or a SO2 group and A denotes hydrogen, an optionally substituted alkoxy or alkenyloxy group, halogen or a group --CH2 Y, in which Y represents hydrogen, halogen or the radical of a nucleophilic compound, and in which the R2 O group is in the syn-position, which compounds are valuable chemotherapeutic agents having a very powerful antimicrobial action against Gram-positive and Gram-negative bacteria and an unexpectedly good action against penicillinase-forming Staphilococci.

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