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63508-56-5

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63508-56-5 Usage

Physical form

Yellow crystalline solid

Type of compound

Derivative of phenazine

Use as a chemical intermediate

Synthesis of pharmaceuticals and agrochemicals

Antimicrobial properties

Useful in the development of antimicrobial agents

Antifungal properties

Useful in the development of antifungal agents

Potential biological activities

Anticancer and antioxidant properties

Industries of use

Pharmaceutical and agricultural industries

Check Digit Verification of cas no

The CAS Registry Mumber 63508-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,0 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63508-56:
(7*6)+(6*3)+(5*5)+(4*0)+(3*8)+(2*5)+(1*6)=125
125 % 10 = 5
So 63508-56-5 is a valid CAS Registry Number.

63508-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-methylphenazin-2-one

1.2 Other means of identification

Product number -
Other names 10-methyl-10H-phenazin-2-one

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:63508-56-5 SDS

63508-56-5Downstream Products

63508-56-5Relevant articles and documents

Hydrobromic acid-dimethyl sulfoxide reagent for dealkylation of 5,10-dialkyl-5,10-dihydrophenazines: Synthesis of 10-alkyl- 2(10H)-phenazinones

Sugimoto, Akira,Yoshino, Yasuyuki,Watanabe, Ryo,Mizuno, Kazuhiko,Uehara, Kaku

, p. 1057 - 1064 (2007/10/03)

By the reaction of 5,10-dialkyl-substituted 5,10- dihydrophenazine with hydrobromic acid in dimethyl sulfoxide at 90-110°, 10-alkyl-2(10H)-phenazinone was obtained as a major product. Brominated dihydrophenazine was isolated in the case of 1,6-dichloro-5,10-dimethyl-5,10-dihydrophenazine.

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