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2-(2,6-Dimethylphenoxy)acetonitrile is an organic compound with the chemical formula C10H11NO. It is a derivative of acetonitrile, featuring a 2,6-dimethylphenoxy group attached to the acetonitrile molecule. 2-(2,6-DiMethylphenoxy)acetonitrile is characterized by its aromatic ring structure, with two methyl groups at the 2nd and 6th positions, and a nitrile group (-CN) at the 2nd position of the phenoxy group. It is a colorless to pale yellow liquid with a molecular weight of 163.20 g/mol. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Due to its reactivity and potential applications, it is important to handle 2-(2,6-dimethylphenoxy)acetonitrile with care, as it may have toxicological properties and should be used in accordance with safety guidelines.

2319-90-6

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2319-90-6 Usage

Common uses

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Functional group

Nitrile (carbon triple-bonded to a nitrogen atom)

Role in organic chemistry

Building block and precursor for the formation of more complex molecules

Value

Versatile and reactive, valuable for research and industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 2319-90-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2319-90:
(6*2)+(5*3)+(4*1)+(3*9)+(2*9)+(1*0)=76
76 % 10 = 6
So 2319-90-6 is a valid CAS Registry Number.

2319-90-6SDS

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 (2,6-dimethylphenoxy)acetonitrile

1.2 Other means of identification

Product number -
Other names 2-(2,6-DIMETHYLPHENOXY)ACETONITRILE

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:2319-90-6 SDS

2319-90-6Relevant academic research and scientific papers

Cytosine analogues from substituted acetonitriles via Thorpe condensation

Barkin, Julia L.,Faust Jr., Marcus D.,Trenkle, William C.

, p. 3333 - 3335 (2007/10/03)

(Matrix presented) A Thorpe condensation is the key bond construction in a rapid and efficient synthesis of substituted cytosine derivatives from readily available starting materials.

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