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16754-86-2

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16754-86-2 Usage

General Description

The chemical compound "(2R,4R,5R)-2-(hydroxymethyl)-5-(5-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraen-9-yl)oxolane-3,4-diol" is a complex molecule composed of a sugar-like structure and a tricyclic component containing a sulfur atom. It has a stereochemistry denoted by the (2R,4R,5R) prefix, indicating the configuration of its chiral centers. The presence of the hydroxymethyl group and the oxolane-3,4-diol moiety suggests potential reactivity with other biomolecules, while the tricyclic portion may impart specific pharmacological properties. The compound's intricate structure, characterized by both its sugar and tricyclic components, may indicate its potential use in medicinal chemistry or as a synthetic building block.

Check Digit Verification of cas no

The CAS Registry Mumber 16754-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,5 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16754-86:
(7*1)+(6*6)+(5*7)+(4*5)+(3*4)+(2*8)+(1*6)=132
132 % 10 = 2
So 16754-86-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H15N3O4S/c1-20-11-6-2-3-15(10(6)13-5-14-11)12-9(18)8(17)7(4-16)19-12/h2-3,5,7-9,12,16-18H,4H2,1H3

16754-86-2SDS

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 2-(hydroxymethyl)-5-(4-methylsulfanylpyrrolo[2,3-d]pyrimidin-7-yl)oxolane-3,4-diol

1.2 Other means of identification

Product number -
Other names -

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

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More Details:16754-86-2 SDS

16754-86-2Downstream Products

16754-86-2Relevant articles and documents

Synthesis, cytostatic, antimicrobial, and anti-HCV activity of 6-substituted 7-(het)aryl-7-deazapurine ribonucleosides

Nau?, Petr,Caletková, Olga,Kone?ny, Petr,D?ubák, Petr,Bogdanová, Kate?ina,Kolá?, Milan,Vrbková, Jana,Slavětínská, Lenka,Tlou?t'Ová, Eva,Perlíková, Pavla,Hajdúch, Marián,Hocek, Michal

, p. 1097 - 1110 (2014/03/21)

A series of 80 7-(het)aryl- and 7-ethynyl-7-deazapurine ribonucleosides bearing a methoxy, methylsulfanyl, methylamino, dimethylamino, methyl, or oxo group at position 6, or 2,6-disubstituted derivatives bearing a methyl or amino group at position 2, were

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