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4-[4-[1-(E)-propenyl]cyclohexyl]-, trans-Benzonitrile, commonly known as Trans-Benzonitrile, is a colorless liquid chemical compound with the molecular formula C14H15N. It possesses an aroma reminiscent of bitter almonds and features a trans configuration, with a cyclohexyl group attached to a benzene ring and a propenyl side chain. Due to its potential hazards upon ingestion, inhalation, or skin absorption, it is crucial to handle 4-[4-[1-(E)-propenyl]cyclohexyl]-, trans-Benzonitrile with care, using appropriate personal protective equipment and ensuring a well-ventilated environment during its use.

96184-40-6

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96184-40-6 Usage

Uses

Used in Pharmaceutical Industry:
Trans-Benzonitrile is utilized as a key building block in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, Trans-Benzonitrile serves as an essential component in the production of various agrochemicals. Its incorporation aids in the development of effective pesticides, herbicides, and other agricultural chemicals that enhance crop protection and yield.
Used in Organic Compounds Synthesis:
Trans-Benzonitrile is also employed as a versatile intermediate in the synthesis of other organic compounds. Its reactive sites and functional groups make it a valuable precursor for the production of specialty chemicals, fragrances, and dyes.
Safety Precautions:
When working with Trans-Benzonitrile, it is imperative to adhere to safety protocols to minimize health risks. This includes wearing appropriate personal protective equipment, such as gloves, goggles, and respirators, and ensuring proper ventilation to prevent inhalation of vapors. Additionally, spills should be promptly cleaned up, and any contaminated materials should be disposed of according to local regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 96184-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,8 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96184-40:
(7*9)+(6*6)+(5*1)+(4*8)+(3*4)+(2*4)+(1*0)=156
156 % 10 = 6
So 96184-40-6 is a valid CAS Registry Number.

96184-40-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-{trans-4-[(1E)-1-Propen-1-yl]cyclohexyl}benzonitrile

1.2 Other means of identification

Product number -
Other names Merphalan

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:96184-40-6 SDS

96184-40-6Downstream Products

96184-40-6Relevant academic research and scientific papers

Liquid crystals

-

, (2008/06/13)

Compounds of the formula STR1 wherein n stands for the number 0 or 1; the rings A1, A2 and A3 represent 1,4-phenylene, 2-fluoro-1,4-phenylene or trans-1,4-cyclohexylene or one of these rings also represents a 2,5-disubstituted pyrimidine ring or a trans-2,5-disubstituted m-dioxane ring; X1 represents a single covalent bond, --COO--, --OOC--, --CH2 CH2 --, p--C6 H4 --, --CH2 CH2 --p-- C6 H4 --, --CH2 CH2 --p--C6 H4 --CH2 CH2 -- or, insofar as the rings A1 and A2 represent 1,4-phenylene, also --NON--; R2 represents 1E-alkenyl, 2Z-alkenyl, 3E-alkenyl, 4-alkenyl or alkenyloxy, with the proviso that the oxygen atom in alkenyloxy is linked with a saturated carbon atom; and R1 signifies 1E-alkenyl, 2Z-alkenyl, 3E-alkenyl, 4-alkenyl or, insofar as R2 represents alkenyloxy, also alkyl, their manufacture, as well as liquid crystalline mixtures and the use for electro-optical purposes.

New Liquid Crystals: The Synthesis and Mesomorphic Properties of Nematic Alkenylsubstituted Cyanophenylcyclohexanes

Petrzilka, Martin

, p. 109 - 124 (2007/10/02)

18 Alkenylsubstituted cyanophenylcyclohexanes have been synthesized by systematically varying both the position and the configuration of the isolated C,C-double bond.The influences of such structural changes on the mesomorphic properties are discussed and

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