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3-(3,4-dimethoxyphenyl)-2-methyl-6-oxohexane-3-carbonitrile is a chemical compound characterized by the presence of a nitrile functional group, a benzene ring with two methoxy substituents, a ketone group, and a methyl group attached to a six-carbon chain. This unique structure endows the compound with potential biological activities, making it a valuable building block for the synthesis of complex organic molecules and new chemical entities with potential applications in the pharmaceutical and agrochemical industries.

27339-25-9

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27339-25-9 Usage

Uses

Used in Pharmaceutical Industry:
3-(3,4-dimethoxyphenyl)-2-methyl-6-oxohexane-3-carbonitrile is used as an intermediate in the synthesis of pharmaceutical compounds for its potential medicinal properties. Its unique structure and functional groups contribute to the development of new drugs with therapeutic benefits.
Used in Agrochemical Industry:
3-(3,4-dimethoxyphenyl)-2-methyl-6-oxohexane-3-carbonitrile is used as a precursor in the production of agrochemicals, such as pesticides and herbicides, due to its potential biological activities against pests and weeds.
Used in Material Science:
3-(3,4-dimethoxyphenyl)-2-methyl-6-oxohexane-3-carbonitrile may have potential applications in the development of new materials, such as polymers and composites, owing to its unique structure and functional groups.
Used in Chemical Synthesis Processes:
3-(3,4-dimethoxyphenyl)-2-methyl-6-oxohexane-3-carbonitrile serves as a valuable building block for the synthesis of complex organic molecules and new chemical entities, contributing to the advancement of chemical synthesis processes and the discovery of novel compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 27339-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,3 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27339-25:
(7*2)+(6*7)+(5*3)+(4*3)+(3*9)+(2*2)+(1*5)=119
119 % 10 = 9
So 27339-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H21NO3/c1-12(2)16(11-17,8-5-9-18)13-6-7-14(19-3)15(10-13)20-4/h6-7,9-10,12H,5,8H2,1-4H3

27339-25-9SDS

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-(3,4-dimethoxyphenyl)-5-oxo-2-propan-2-ylpentanenitrile

1.2 Other means of identification

Product number -
Other names EINECS 248-416-3

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:27339-25-9 SDS

27339-25-9Relevant academic research and scientific papers

PROCESS FOR PREPARING N-METHYL-3, 4-DIMETHOXYPHENYLETHYLAMINE

-

Page/Page column 6, (2009/07/17)

Provided are intermediates useful for the preparation of verapamil and methods for their preparation.

SOME NEW ANALOGUES OF VERAPAMIL AND MEPAMIL. SYNTHESIS AND BASIC PHARMACOLOGICAL PROPERTIES

Butora, Gabriel,Blaha, Ludvik,Rajsner, Miroslav,Helfert, Ivan

, p. 1967 - 1981 (2007/10/02)

Some new analogues of verapamil (Ia) and mepamil (Ib), calcium antagonists of arylkylamine type, were synthesized and screened for cardiovascular activities.The basic structure was modified a) on the phenyl ring, attached to the quaternary carbon, b) on the alkyl group, attached to the quaternary carbon and c) on the alkylamino group, attached in position 3 to the n-propyl fragment.Except of 2-(2-chlorophenyl)-2-isopropyl-5-(N-methylhomoveratrylamino)valeronitrile (VIa), all the synthesized compounds exhibited lower hypotensive activity, than the mother compound, verapamil.

Tetrahydroisoquinoline derivatives

-

, (2008/06/13)

Compounds of the formula STR1 wherein R1 and R2 and each independently --H or lower alkoxy; R3 and R4 are each independently lower alkyl; and R5 and R6 are each --OCH3, or together form --OCH2 O-- or --OCH2 CH2 O--, and pharmaceutically acceptable acid addition salts thereof are prepared by cyclizing, deoxygenating, coupling, or hydrogenating the intermediates disclosed herein.

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