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870704-27-1

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870704-27-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 870704-27-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,7,0 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 870704-27:
(8*8)+(7*7)+(6*0)+(5*7)+(4*0)+(3*4)+(2*2)+(1*7)=171
171 % 10 = 1
So 870704-27-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H4ClNO3/c6-1-4-3(5(8)9)2-7-10-4/h2H,1H2,(H,8,9)

870704-27-1 Well-known Company Product Price

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  • Aldrich

  • (644765)  5-(Chloromethyl)isoxazole-4-carboxylicacid  97%

  • 870704-27-1

  • 644765-1G

  • 1,062.36CNY

  • Detail
  • Aldrich

  • (644765)  5-(Chloromethyl)isoxazole-4-carboxylicacid  97%

  • 870704-27-1

  • 644765-5G

  • 3,690.18CNY

  • Detail

870704-27-1SDS

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 5-(chloromethyl)-1,2-oxazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-CHLOROMETHYL-ISOXAZOLE-4-CARBOXYLIC ACID

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:870704-27-1 SDS

870704-27-1Downstream Products

870704-27-1Relevant articles and documents

Stereoselective synthesis of novel uracil polyoxin C conjugates as substrate analogues of chitin synthase

Plant, Andrew,Thompson, Peter,Williams, David M.

, p. 3714 - 3724 (2008/09/19)

(Chemical Equation Presented) Stereoselective syntheses of both the natural (C5′-S) and unnatural (C5′-R) diastereoisomers of uracil polyoxin C methyl ester have been developed. The key stereocontrolled step involves nucleophilic addition of trimethylsily

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