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102569-26-6

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102569-26-6 Usage

General Description

2-Amino-4-hydroxy-3-methylbenzonitrile is a chemical compound that belongs to the class of benzonitriles. It has a molecular formula C8H8N2O and a molecular weight of 148.16 g/mol. It is known for its role in the synthesis of pharmaceuticals, particularly in the development of various drugs. Additionally, it is utilized in the production of dyes and other organic compounds. The compound is notable for its potential therapeutic applications, and its structure and properties make it a valuable component in medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 102569-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,6 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102569-26:
(8*1)+(7*0)+(6*2)+(5*5)+(4*6)+(3*9)+(2*2)+(1*6)=106
106 % 10 = 6
So 102569-26-6 is a valid CAS Registry Number.

102569-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-4-hydroxy-3-methylbenzonitrile

1.2 Other means of identification

Product number -
Other names Benzonitrile,2-amino-4-hydroxy-3-methyl

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:102569-26-6 SDS

102569-26-6Relevant articles and documents

Macrocylic Inhibitors of Hepatitis C Virus

-

, (2009/05/28)

Compounds of the formula I: and N-oxides, salts, and stereoisomers thereof wherein A is OR1, NHS(═O)pR2; wherein; R1 is hydrogen, C1-C6alkyl, C0-C3alkylenecarbocyclyl, C0-C3alkylene-heterocyclyl;R2 is C1-C6alkyl, C0-C3alkylenecarbocyclyl, C0-C3alkyleneheterocyclyl;p is independently 1 or 2;n is 3, 4, 5 or 6; — denotes an optional double bond;L is N or CRz; Rz is H or forms a double bond with the asterisked carbon;Rq is H or when L is CRz, Rq can also be C1-C6alkyl;Rr is quinazolinyl, optionally substituted with one two or three substituents each independently selected from C1-C6 alkyl, C1-C6alkoxy, hydroxyl, halo, haloC1-C6alkyl, amino, mono- or dialkylamino, mono- or dialkylaminocarbonyl, C1-C6alkyl-carbonylamino, C0-C3alkylenecarbocyclyl and C0-C3 alkyleneheterocyclyl;R5 is hydrogen, C1-C6alkyl, C1-C6alkoxyC1-C6alkyl or C3-C7cycloalkyl;R6 is hydrogen, C1-C6alkyl, C1-C6alkoxy, C0-C3alkylenecarbocyclyl, C0-C3alkylene-heterocyclyl, hydroxy, bromo, chloro or fluoro have utility in the treatment or prophylaxis of flaviviral infections such as HCV

Einfache Synthese neuer 2-Amino-4-hydroxybenzonitrile

Schmidt, Hans-Werner

, p. 778 - 779 (2007/10/02)

4-Aminosalicylic acid derivatives are decarboxylated to the 2-amino-4-hydroxybenzonitriles 2 by heating in quinoline at 170-180 deg C.The bromo and iodo derivatives of 2 are prepared by nuclear bromination and reaction with iodine in the presence of iodic

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