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67341-53-1

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67341-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67341-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,4 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67341-53:
(7*6)+(6*7)+(5*3)+(4*4)+(3*1)+(2*5)+(1*3)=131
131 % 10 = 1
So 67341-53-1 is a valid CAS Registry Number.

67341-53-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-3-phenyl-1H-pyrazin-2-one

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-3-phenyl-6-methylpyrazin

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:67341-53-1 SDS

67341-53-1Relevant articles and documents

2-Hydroxy-3-aryl-6-methylpyrazines; fluorophores formed from the reaction of formaldehyde with cyclic enamine degradation products common to β-lactam antibiotics with aryl glycine side chains

Indelicato,Dorman,Engel

, p. 119 - 121 (2007/10/02)

-

Isolation and identification of the fluorescent degradation product of some β-lactam antibiotics

Barbhaiya,Brown,Payling,Turner

, p. 224 - 227 (2007/10/10)

A fluorescent degradation product of cephalexin, recently employed in the determination of this antibiotic in aqueous solution and human plasma, has been isolated and identified as 2-hydroxy-3-phenyl-6-methylpyrazine. Spectroscopically and chromatographically the product is indistinguishable from that obtained by the same method from a series of other cephalosporins and penicillins bearing an α-amino group on the side-chain, and from the pyrazine structure produced by synthesis. Two reported methods for the fluorimetric determination of ampicillin have also been found to yield the same degradation product and not the suggested diketopiperazine structure.

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