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86137-72-6

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86137-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86137-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,3 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86137-72:
(7*8)+(6*6)+(5*1)+(4*3)+(3*7)+(2*7)+(1*2)=146
146 % 10 = 6
So 86137-72-6 is a valid CAS Registry Number.

86137-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2'-deoxy-O6-[2-(4-nitrophenyl)ethyl]guanosine

1.2 Other means of identification

Product number -
Other names 2'-DEOXY-6-O-[2-(4-NITROPHENYL)ETHYL]GUANOSINE

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:86137-72-6 SDS

86137-72-6Relevant articles and documents

Synthesis and evaluation of pyrrole polyamide-2′-deoxyguanosine 5′-phosphate hybrid

Kawashima, Etsuko,Nakanishi, Yasuhiro,Terui, Yusuke,Tomitori, Hideyuki,Kashiwagi, Keiko,Ohba, Yusuke,Kamaike, Kazuo

, p. 196 - 205 (2013/06/04)

Pyrrole polyamide-2′-deoxyguanosine 5′-phosphate hybrid (Hybrid 4) was synthesized and evaluated in terms of the inhibition of mouse mammary carcinoma FM3A cell growth. Hybrid 4 was found to exhibit dose-dependent inhibition of cell growth.

Nucleotides: Part LXI: Phthaloyl strategy: A new concept of oligonucleotide synthesis

Beier, Markus,Pfleiderer, Wolfgang

, p. 633 - 644 (2007/10/03)

A new alternative strategy of oligonucleotide synthesis was developed by use of the phthaloyl protecting group for the exocyclic amino functions of the nucleobases (see 9-12). This approach combines the advantages of cheap and easily accessible monomeric building blocks (see 17- 20), standard machine-aided oligonucleotide synthesis, and a fast deprotection protocol which is orthogonal to the cleavage procedure from the solid support. The crude oligonucleotides show high purity and require, in general, no further chromatographic purification.

Synthesis of Oligonucleotide Adducts of the Bay Region Diol Epoxide Metabolites of Carcinogenic Polycyclic Aromatic Hydrocarbons

Lee, Hongmee,Luna, Ernestina,Hinz, Michael,Stezowski, John J.,Kiselyov, Alexander S.,Harvey, Ronald G.

, p. 5604 - 5613 (2007/10/03)

An efficient method for the site-specific synthesis of adducts between the biologically active diol epoxide metabolites of carcinogenic polycyclic aromatic hydrocarbons (PAHs) and oligonucleotides in which a PAH component of predetermined stereochemistry

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