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Benzonitrile, 2-amino-4-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67608-59-7

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67608-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67608-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,0 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 67608-59:
(7*6)+(6*7)+(5*6)+(4*0)+(3*8)+(2*5)+(1*9)=157
157 % 10 = 7
So 67608-59-7 is a valid CAS Registry Number.

67608-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-4-hydroxy-benzonitril

1.2 Other means of identification

Product number -
Other names 3-amino-4-cyanophenol

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:67608-59-7 SDS

67608-59-7Relevant academic research and scientific papers

SULPHOXIMINE-SUBSTITUTED QUINAZOLINE DERIVATIVES AS IMMUNO-MODULATORS, THEIR PREPARATION AND USE AS MEDICAMENTS

-

Page/Page column 36, (2009/07/25)

The present invention relates to sulphoximine-substituted quinazoline derivatives of the formula (I), processes for their preparation and their use as a medicament for the treatment of various diseases.

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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