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3066-84-0

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3066-84-0 Usage

General Description

8-Bromoguanine is a chemical compound that is derived from guanine, one of the four main nucleobases found in the nucleic acids DNA and RNA. It is created through the process of bromination, where a bromine atom replaces one of the hydrogen atoms in the guanine molecule. It is a photosensitizer, meaning it can absorb light and transfer that energy to other molecules. In molecular biology, 8-Bromoguanine is used primarily as a mutagen, a compound that can induce genetic mutation. This makes it a valuable tool in genetic research. However, due to its mutagenic properties, it also poses potential risks, particularly in relation to the toxicity and carcinogenicity.

Check Digit Verification of cas no

The CAS Registry Mumber 3066-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3066-84:
(6*3)+(5*0)+(4*6)+(3*6)+(2*8)+(1*4)=80
80 % 10 = 0
So 3066-84-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H4BrN5O/c6-4-8-1-2(9-4)10-5(7)11-3(1)12/h1H,(H3,7,8,9,10,11,12)

3066-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-8-bromo-3,7-dihydropurin-6-one

1.2 Other means of identification

Product number -
Other names 8-bromo-2-aminohypoxanthine

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:3066-84-0 SDS

3066-84-0Relevant articles and documents

Hydrolysis of 2'-Deoxypurine Nucleosides. The Effect of Substitution at the C-8 Position.

Laayoun, Ali,Decout, Jean-Luc,Lhomme, Jean

, p. 4989 - 4990 (2007/10/02)

The hydrolytic stability of 2'-deoxypurine nucleosides is decreased by introduction of electronwithdrawing substituents at the C-8 position in the series of compounds 2-8, 10-14.The sulfone group causes a 2.9 x 104 rate acceleration for glycosidic, bond cleavage in compound 14.

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