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7-(3-carboxy-5-hydroxy-3,4-dihydro-2H-1,4-benzothiazinyl)alanine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30612-54-5

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30612-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30612-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,1 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30612-54:
(7*3)+(6*0)+(5*6)+(4*1)+(3*2)+(2*5)+(1*4)=75
75 % 10 = 5
So 30612-54-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O5S/c13-6(11(16)17)1-5-2-8(15)10-9(3-5)20-4-7(14-10)12(18)19/h2-3,6-7,14-15H,1,4,13H2,(H,16,17)(H,18,19)

30612-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(2-amino-2-carboxyethyl)-5-hydroxy-3,4-dihydro-2H-1,4-benzothiazine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 7-DBA

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:30612-54-5 SDS

30612-54-5Upstream product

30612-54-5Downstream Products

30612-54-5Relevant academic research and scientific papers

Characterisation of 1,4-benzothiazine intermediates in the oxidative conversion of 5-S-cysteinyldopa to pheomelanins

Napolitano, Alessandra,Costantini, Claudio,Crescenzi, Orlando,Prota, Giuseppe

, p. 6365 - 6368 (1994)

Under biologically relevant conditions, oxidation of 5-S-cysteinyldopa (1) pheomelanins proceeds through the formation of the 1,4-benzothiazine 7 along with the 3-carboxy analogue 6 in much smaller amounts, as evidenced by isolation of the reduced forms 5 and 4 and by deuterium labelling experiments.

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