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139743-08-1

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139743-08-1 Usage

General Description

(2-AMINO-3-NITRO-PHENYL)-METHANOL is a chemical compound with the molecular formula C7H8N2O4. It is a derivative of phenol with a nitro and an amino group attached to the aromatic ring. (2-AMINO-3-NITRO-PHENYL)-METHANOL is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. It is known for its potential applications in the field of medicinal chemistry and organic synthesis. Additionally, (2-AMINO-3-NITRO-PHENYL)-METHANOL is also used as a reagent in chemical reactions and as a building block for the preparation of more complex organic molecules. Its structure and properties make it a versatile compound with diverse potential uses in different branches of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 139743-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,7,4 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 139743-08:
(8*1)+(7*3)+(6*9)+(5*7)+(4*4)+(3*3)+(2*0)+(1*8)=151
151 % 10 = 1
So 139743-08-1 is a valid CAS Registry Number.

139743-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-amino-3-nitrophenyl)methanol

1.2 Other means of identification

Product number -
Other names 2-Amino-3-nitrobenzenemethanol

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:139743-08-1 SDS

139743-08-1Relevant articles and documents

2-Phenyl-4-piperazinylbenzimidazoles: Orally active inhibitors of the gonadotropin releasing hormone (GnRH) receptor

Pelletier, Jeffrey C.,Chengalvala, Murty,Cottom, Josh,Feingold, Irene,Garrick, Lloyd,Green, Daniel,Hauze, Diane,Huselton, Christine,Jetter, James,Kao, Wenling,Kopf, Gregory S.,Lundquist IV, Joseph T.,Mann, Charles,Mehlmann, John,Rogers, John,Shanno, Linda,Wrobel, Jay

, p. 6617 - 6640 (2008/12/22)

Antagonism of the gonadotropin releasing hormone (GnRH) receptor has shown positive clinical results in numerous reproductive tissue disorders such as endometriosis, prostate cancer and others. Traditional therapy has been limited to peptide agonists and

Imidazo[1,5-A]quinoxalines

-

, (2008/06/13)

An invention relating to Imidazo[1,5-a]quinoxalines (I) STR1 which do not contain an endocyclic carbonyl group and which are useful as anxiolytic and sedative/hypnotic agents.

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