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37987-22-7

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37987-22-7 Usage

Chemical Structure

Contains a benzene ring substituted with a hydroxyl group, a methoxy group, and a nitro group at specific positions.

Functionality

Nitrophenol derivative

Primary Uses

Convulsant
Insecticide

Mode of Action

Acts as a potent antagonist of the gamma-aminobutyric acid (GABA) receptor.

Research Applications

Studying the effects of GABA on the central nervous system
Investigating potential medicinal properties, including:
Treatment of drug addiction
Management of neurological disorders such as epilepsy

Check Digit Verification of cas no

The CAS Registry Mumber 37987-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,8 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 37987-22:
(7*3)+(6*7)+(5*9)+(4*8)+(3*7)+(2*2)+(1*2)=167
167 % 10 = 7
So 37987-22-7 is a valid CAS Registry Number.

37987-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(hydroxymethyl)-2-methoxy-6-nitrophenol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,4-hydroxy-3-methoxy-5-nitro

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:37987-22-7 SDS

37987-22-7Relevant articles and documents

Annulation-Induced Cascade Transformation of 5-Iodo-1,2,3-triazoles to 2-(1-Aminoalkyl)benzoxazoles

Kotovshchikov, Yury N.,Latyshev, Gennadij V.,Navasardyan, Mger A.,Erzunov, Dmitry A.,Beletskaya, Irina P.,Lukashev, Nikolay V.

supporting information, p. 4467 - 4470 (2018/08/09)

Base-mediated cyclization of (5-iodo-1,2,3-triazolyl)phenols was proposed as a new synthetic strategy for the in situ generation of diazoimines via electrocyclic ring opening of the fused heterocycle. Cu-catalyzed amination of the intermediate diazoalkanes was employed to develop an efficient cascade approach to functionalized benzoxazoles.

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