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64060-84-0

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64060-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64060-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,6 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64060-84:
(7*6)+(6*4)+(5*0)+(4*6)+(3*0)+(2*8)+(1*4)=110
110 % 10 = 0
So 64060-84-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H13N5O10P2/c11-9-8-10(13-4-12-9)15(5-14-8)7(2-17)24-6(1-16)3-23-27(21,22)25-26(18,19)20/h1-2,4-7H,3H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t6-,7+/m0/s1

64060-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R)-2-[(1R)-1-(6-aminopurin-9-yl)-2-oxoethoxy]-3-oxopropyl] phosphono hydrogen phosphate

1.2 Other means of identification

Product number -
Other names Diphosphoric acid mono(2-(1-(6-amino-9H-purin-9-yl)-2-oxoethoxy)-3-oxopropyl)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:64060-84-0 SDS

64060-84-0Upstream product

64060-84-0Downstream Products

64060-84-0Relevant articles and documents

BOROHYDRIDE REDUCTION OF PERIODATE-OXIDIZED NUCLEOTIDES; ISOLATION AND STRUCTURE OF THE REDUCTION INTERMEDIATE

Rosenthal, Luann P.,Hogenkamp, Harry P. C.,Bodley, James W.

, p. 85 - 92 (1982)

The reduction of periodate-oxidized nucleotides with sodium borohydride proceeds via a reaction intermediate presumed to be a monoalcohol.The borohydride-reduction intermediate of periodate-oxidized ADP has been isolated by anionexchange, liquid chromatography, and subjected to further reduction.Using sodium borohydride and sodium borodeuteride alternately in the two reduction steps, it was determined, by 1H-n.m.r.-spectral analysis, that the two aldehyde groups are sequentially reduced in the order 3' and 2', and it was concluded that the isolated intermediate corresponds to the semi-reduced, 3'-alcohol, 2'-aldehyde derivative.This compound should be a useful analog for the study of enzymes and proteins that interact with nucleotides.

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