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340131-70-6

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340131-70-6 Usage

General Description

2-hydroxy-3-tert-butyl benzonitrile is a chemical compound with the molecular formula C14H17NO. It is an aromatic compound with a hydroxyl group and a tert-butyl group attached to a benzonitrile ring. This chemical is used in the fragrance and flavor industry as a synthetic musk with a sweet, floral odor. It is also used as a fragrance ingredient in various cosmetic and personal care products. 2-hydroxy-3-tert-butyl benzonitrile may have potential health effects, and precautions should be taken when handling and using this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 340131-70-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,0,1,3 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 340131-70:
(8*3)+(7*4)+(6*0)+(5*1)+(4*3)+(3*1)+(2*7)+(1*0)=86
86 % 10 = 6
So 340131-70-6 is a valid CAS Registry Number.

340131-70-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-3-tert-butyl benzonitrile

1.2 Other means of identification

Product number -
Other names 3-(tert-Butyl)-2-hydroxybenzonitrile

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:340131-70-6 SDS

340131-70-6Relevant articles and documents

A one-pot synthesis of substituted salicylnitriles

Anwar, Hany F.,Hansen, Trond Vidar

, p. 4443 - 4445 (2008)

Phenols were converted to salicylaldehydes with paraformaldehyde, MgCl2-Et3N in THF, and subsequent treatment with aqueous ammonia gave the corresponding imines which were oxidized with IBX to the desired salicylnitriles. The sequence of reactions was conveniently carried out as a one-pot procedure under mild conditions.

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