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42241-07-6

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42241-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42241-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,4 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42241-07:
(7*4)+(6*2)+(5*2)+(4*4)+(3*1)+(2*0)+(1*7)=76
76 % 10 = 6
So 42241-07-6 is a valid CAS Registry Number.

42241-07-6SDS

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 7-chloro-5,10-dihydro-4H-thieno[3,2-c][1]benzazepin-4-one

1.2 Other means of identification

Product number -
Other names 7-chloro-5,10-dihydro-benzo[b]thieno[2,3-e]azepin-4-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:42241-07-6 SDS

42241-07-6Upstream product

42241-07-6Relevant articles and documents

A New Oxidation Pathway of the Neurotoxin 6-Aminodopamine. Isolation and Characterisation of a Dimer with a Tetrahydroiminoethanophenoxazine Ring System.

Napolitano, Alessandra,d'Ischia, Marco,Costantini, Claudio,Prota, Giuseppe

, p. 8515 - 8522 (2007/10/02)

Oxidation of the neurotoxin 6-aminodopamine (1) is known to proceed through the o-quinone 3, which undergoes intramolecular cyclisation to give 5,6-dihydroxyindole (6).In a re-examination of the reaction, we have found that at concentrations of 1 higher than 5 * 10-3 M a quite different course prevails, leading to the formation of the novel 7-amino-8-(2-aminoethyl)-3-hydroxy-2-oxo-2,3,4,10-tetrahydroiminoethanophenoxazine (7).Product 7 was formed by aerobic, chemical (persulphate, periodate) or enzymatic (tyrosinase, peroxidase/H2O2) oxidation of 1.On acetylation, 7 afforded the tetraacetate 8.Oxidation of the model compound 5-amino-4-methylcatechol (9) proceeded similarly as that of 1, to give the tetrahydrophenoxazinedione 11.

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