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2962-89-2

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2962-89-2 Usage

Classification

Chemical compound

Group

Pteridine group of compounds

Natural Occurrence

Commonly found in nature

Synthesis

Can be synthesized in the laboratory

Antioxidant

Has antioxidant properties

Photo-protective

Provides protection against harmful effects of light

Medical

Studied for potential use in treating certain diseases and conditions

Cosmetic

Used as a skin-lightening agent

Intermediate

Used in the synthesis of other compounds

Dietary Supplements

Can be found in some dietary supplements

Stability

Relatively stable compound

Toxicity

Low toxicity, making it a desirable ingredient for various applications

Check Digit Verification of cas no

The CAS Registry Mumber 2962-89-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2962-89:
(6*2)+(5*9)+(4*6)+(3*2)+(2*8)+(1*9)=112
112 % 10 = 2
So 2962-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H11N4O3/c1-14-10-9(11(17)15(2)12(14)18)16(19)8-6-4-3-5-7(8)13-10/h3-6,9H,1-2H3/q+1

2962-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethyl-5-oxidobenzo[g]pteridin-5-ium-2,4-dione

1.2 Other means of identification

Product number -
Other names Alloxazine,3-dimethyl-,5-oxide

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:2962-89-2 SDS

2962-89-2Downstream Products

2962-89-2Relevant articles and documents

New Synthesis of Alloxazine Derivatives

Krasnov

, p. 115 - 119 (2007/10/03)

Nitrosation of 6-anilino-1,3-dimethyluracils yields 1,3-dimethylalloxazine derivatives and the corresponding 5-oxides. Reduction of the N-oxides results in formation of the alloxazines. This reaction opens the way to difficultly accessible alloxazine deri

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