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55781-71-0

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55781-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55781-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,8 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55781-71:
(7*5)+(6*5)+(5*7)+(4*8)+(3*1)+(2*7)+(1*1)=150
150 % 10 = 0
So 55781-71-0 is a valid CAS Registry Number.

55781-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-CHLORO-5-AMINO-3-PICOLINE

1.2 Other means of identification

Product number -
Other names 6-Chloro-5-methyl-3-pyridinamine

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:55781-71-0 SDS

55781-71-0Upstream product

55781-71-0Downstream Products

55781-71-0Relevant articles and documents

Purines, Pyrimidines and Imidazoles. Part 55. Some D-Lyxofuranosyl Imidazoles Related to Intermediates in Purine Nucleotide de novo biosynthesis.

Mackensie, Grahame,Shaw, Gordon

, p. 3201 - 3228 (2007/10/02)

Ethyl 5-N-acetylamino-1-(2,3:5,6-di-O-isopropylidene-α- and -β-D-mannofuranosyl)imidazole-4-carboxylates prepared by acetylation of the corresponding 5-amino derivatives and methanolysis of the mixture of 5-N-mono- and di-acetylaminoimidazoles produced were converted by aqueous acetic acid into ethyl 5-N-acetylamino 1-(2,3-O-isopropylidene-α- and β-D-mannofuranosyl)imidazole-4-carboxylates which with sodium periodate followed by sodium borohydride gave ethyl 5-N-acetylamino-1-(2,3-O-isopropylidene-α- and -β-D-lyxofuranosyl)imidazole-4-carboxylates.The configurations assigned to the anomeric lyxone nucleosides were confirmed by comparison of specific rotations of glycerol derivatives produced by periodate oxidation of the deacetonated nucleosides with that from an analogous ribose derivative, and by n.m.r. and c.d. studies.Products of acylation of several aminoimidazoles with trifluoroacetic anhydride and acetyl chloride are also described.

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