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10133-36-5

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10133-36-5 Usage

General Description

2-NITRO-BENZO[B]THIOPHEN-3-YLAMINE is a chemical compound with the molecular formula C8H6N2O2S. It is a nitrobenzothiophene derivative, which is often used in pharmaceutical and agrochemical research. The compound has a nitro group and an amine group attached to the benzothiophene ring. It is known for its potential as a building block in the synthesis of various pharmaceutical and agrochemical compounds. The compound is known to have various biological activities and has been studied for its potential medicinal uses. 2-NITRO-BENZO[B]THIOPHEN-3-YLAMINE has also been investigated for its potential as an anti-cancer and anti-inflammatory agent.

Check Digit Verification of cas no

The CAS Registry Mumber 10133-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,3 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10133-36:
(7*1)+(6*0)+(5*1)+(4*3)+(3*3)+(2*3)+(1*6)=45
45 % 10 = 5
So 10133-36-5 is a valid CAS Registry Number.

10133-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Nitro-1-benzothiophen-3-amine

1.2 Other means of identification

Product number -
Other names -

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:10133-36-5 SDS

10133-36-5Downstream Products

10133-36-5Relevant articles and documents

SELECTIVE HDAC1 AND HDAC2 INHIBITORS

-

, (2014/05/20)

Provided herein are compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with HDAC activity, particularly diseases or disorders that involve activity of HDAC1 and/or HDAC2. Such diseases include cancer, sickle-cell anemia, beta-thalassemia, and HIV.

Synthesis of Substituted Benzothienopyrazines

Cannizzo, Sergio,Guerrera, Francesco,Siracusa, Maria Angela,Corsaro, Antonino

, p. 2175 - 2179 (2007/10/02)

The synthesis of a series of novel 1-unsubstituted and 1-alkyl-1,2,3,4-tetrahydrobenzothienopyrazine-2,3-diones 4a-d and their corresponding dialkylaminoalkylamino derivatives 6a-d starting from 2-nitro-3-bromobenzothiophene is described.The

Bromonitromethane, a Versatile Electrophile: Reactions with Thiolates

Fishwick, Brian R.,Rowles, David K.,Stirling, Charles J. M.

, p. 834 - 835 (2007/10/02)

Thiolate ions react with bromonitromethane to give nitronate ion and, initially, sulphenyl bromide which reacts with further thiolate ion to give disulphide; when the disulphide bears an appropriately placed nitrile function, intramolecular attack by the nitronate ion at this function and subsequent intramolecular displacement of thiolate ion yields aminothiophenes.

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