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20503-40-6

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20503-40-6 Usage

General Description

6-AMINO-1H-1LAMBDA6-BENZO[B]THIOPHENE-1,1-DIONE is a chemical compound with the molecular formula C8H5NO2S. It is a heterocyclic compound containing a sulfur atom and a nitrogen atom in the five-membered ring structure. The compound is a derivative of benzo[b]thiophene-1,1-dione and contains an amino group at the 6-position. 6-AMINO-1H-1LAMBDA6-BENZO[B]THIOPHENE-1,1-DIONE has potential applications in the field of organic synthesis and pharmaceutical research due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 20503-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,0 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20503-40:
(7*2)+(6*0)+(5*5)+(4*0)+(3*3)+(2*4)+(1*0)=56
56 % 10 = 6
So 20503-40-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO2S/c9-7-2-1-6-3-4-12(10,11)8(6)5-7/h1-5H,9H2

20503-40-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dioxo-1-benzothiophen-6-amine

1.2 Other means of identification

Product number -
Other names 6-amino-1

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:20503-40-6 SDS

20503-40-6Relevant articles and documents

Synthesis and cytotoxic activity of lipophilic sulphonamide derivatives of the benzo[b]thiophene 1,1-dioxide

Villar,Encio,Migliaccio,Gil,Martinez-Merino

, p. 963 - 968 (2007/10/03)

In the search of new compounds with antineoplastic activity, we have analysed the effect of several structural modifications on the nucleus 6-benzo[b]thiophenesulphonamide 1,1-dioxide on its cytotoxic activity on tumour cells. Lipophilic substituents on t

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