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608537-49-1

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608537-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 608537-49-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,8,5,3 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 608537-49:
(8*6)+(7*0)+(6*8)+(5*5)+(4*3)+(3*7)+(2*4)+(1*9)=171
171 % 10 = 1
So 608537-49-1 is a valid CAS Registry Number.

608537-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Methoxy-N,1-dimethylcyclopropanecarboxamide

1.2 Other means of identification

Product number -
Other names N-Methoxymethylphenobarbitone

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:608537-49-1 SDS

608537-49-1Relevant articles and documents

CYCLOPROPYL ETHYLENE COMPOUND AND ARTHROPOD PEST CONTROL COMPOSITION CONTAINING SAME

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Paragraph 0339-0342; 0344, (2021/02/05)

The present invention provides a compound that have excellent harmful arthropod controlling effects, the compounds being represented by formula (I) [wherein R1 represents a hydrogen atom etc., and R21, R22, R31

INDAZOLES AND AZAINDAZOLES AS LRRK2 INHIBITORS

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Page/Page column 423; 424, (2021/01/29)

The present invention is directed to indazole and azaindazole compounds which are inhibitors of LRRK2 and are useful in the treatment of CNS disorders.

PYRROLOPYRIMIDINE ITK INHIBITORS

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Paragraph 0447; 0448; 0449, (2020/02/27)

Disclosed herein are arylpyridinone compounds and compositions useful in the treatment of ITK mediated diseases, such as inflammation, having the structures of Formulas (I)-(IV): wherein the R groups, m, n, and X are as defined in the detailed description. Methods of inhibition of ITK activity in a human or animal subject are also provided.

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