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3-(3,5-dimethylphenoxy)propanenitrile, also known as 3,5-dimethylphenoxypropanenitrile, is an organic compound with the chemical formula C12H13NO. It is a colorless to pale yellow liquid with a molecular weight of 189.24 g/mol. 3-(3,5-dimethylphenoxy)propanenitrile is characterized by the presence of a nitrile group (-CN) attached to a propene chain, which is further substituted with a 3,5-dimethylphenoxy group. The 3,5-dimethylphenoxy group consists of a benzene ring with two methyl groups at the 3rd and 5th positions, and an ether linkage to the propene chain. This chemical is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain herbicides and insecticides. Its chemical structure and properties make it a versatile building block in the development of various chemical compounds.

3649-02-3

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3649-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3649-02-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,4 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3649-02:
(6*3)+(5*6)+(4*4)+(3*9)+(2*0)+(1*2)=93
93 % 10 = 3
So 3649-02-3 is a valid CAS Registry Number.

3649-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3,5-dimethylphenoxy)propanenitrile

1.2 Other means of identification

Product number -
Other names -

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

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More Details:3649-02-3 SDS

3649-02-3Relevant academic research and scientific papers

Acid activated montmorillonite K-10 mediated intramolecular acylation: Simple and convenient synthesis of 4-chromanones

Begum, Ayisha F.,Balasubramanian, Kalpattu K.,Shanmugasundaram, Bhagavathy

, (2021/09/13)

3-Aryloxyproionic acids undergo intramolecular cyclization in the presence of AA.Mont.K-10 in toluene under reflux for 30–45 min in good to excellent yields. Phenyl ring bearing various substituents at the ortho, meta, para positions undergo this cyclization reaction. This method involves simple work up and amenable for large scale preparations. The heterogeneous acid treated catalyst can be regenerated and used for up to three cycles with minimum loss of activity.

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