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2,4-dimethylcyclohex-3-ene-1-carbonitrile, a chemical compound with the molecular formula C9H13N, is a nitrile derivative of a cyclohexene compound. It features a cyclohexene ring with two methyl groups attached, providing structural diversity and potential for various chemical reactions. 2,4-dimethylcyclohex-3-ene-1-carbonitrile is recognized for its role as an intermediate in the synthesis of organic compounds and pharmaceuticals, as well as its potential applications in organic chemistry and as a building block for complex chemical production. Its possible biological activities also make it a subject of interest for further research and development.

66848-41-7

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66848-41-7 Usage

Uses

Used in Organic Synthesis:
2,4-dimethylcyclohex-3-ene-1-carbonitrile is used as an intermediate in the synthesis of various organic compounds for its ability to participate in a range of chemical reactions due to its nitrile and cyclohexene functionalities.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,4-dimethylcyclohex-3-ene-1-carbonitrile is utilized as a building block for the development of new drugs, leveraging its structural properties to create complex and potentially bioactive molecules.
Used in Organic Chemistry Research:
2,4-dimethylcyclohex-3-ene-1-carbonitrile serves as a subject of interest in organic chemistry research, where its reactivity and potential to form new chemical entities are explored for advancing the field and discovering novel applications.
Used in Chemical Production:
2,4-dimethylcyclohex-3-ene-1-carbonitrile is used as a component in the production of complex chemicals, contributing to the creation of advanced materials and specialty chemicals that require its unique structural attributes.
Used in Biological Research:
Due to its potential biological activities, 2,4-dimethylcyclohex-3-ene-1-carbonitrile is also used in biological research to investigate its interactions with biological systems, which may lead to the discovery of new therapeutic agents or other applications in biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 66848-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,4 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66848-41:
(7*6)+(6*6)+(5*8)+(4*4)+(3*8)+(2*4)+(1*1)=167
167 % 10 = 7
So 66848-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N/c1-7-3-4-9(6-10)8(2)5-7/h5,8-9H,3-4H2,1-2H3

66848-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethylcyclohex-3-ene-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 2,4-Dimethyl-3-cyclohexene-1-carbonitrile

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:66848-41-7 SDS

66848-41-7Downstream Products

66848-41-7Relevant academic research and scientific papers

Ketone precursors for organoleptic compounds

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, (2008/06/13)

The invention discloses ketones of formula I: wherein, Y is an optionally substituted alkyl, cycloalkyl, or cycloalkylalkyl, wherein each alkyl group is straight or branched and each alkyl and cycloalkyl group is saturated or unsaturated; R1is hydrogen or a C1-6alkyl group that is substituted, saturated or unsaturated, straight or branched; A is a chromophoric substituted aromatic ring or ring system; n is an integer; and with the proviso that formula I is not 2-ethoxy-1-phenyl-ethanone. These compositions are useful for the delivery of organoleptic compounds, especially of flavors, fragrances, masking agents and antimicrobial compounds.

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