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93743-04-5

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  • Factory Price OLED 99% 93743-04-5 Benzonitrile,2-fluoro-4-[(trans,trans)-4'-propyl[1,1'-bicyclohexyl]-4-yl]- Manufacturer

    Cas No: 93743-04-5

  • USD $ 0.1-0.1 / Gram

  • 1 Gram

  • 100 Metric Ton/Year

  • Xi'an Xszo Chem Co., Ltd.
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93743-04-5 Usage

Description

2-Fluoro-4-[(trans,trans)-4'-propyl[1,1'-bicyclohexyl]-4-yl]benzonitrile is a complex organic chemical compound characterized by the molecular formula C23H27FN and a molecular weight of 331.47 g/mol. It features a fluoro-substituted benzonitrile ring with a unique trans,trans-4'-propyl[1,1'-bicyclohexyl]-4-yl group attached to it. 2-Fluoro-4-[(trans,trans)-4'-propyl[1,1'-bicyclohexyl]-4-yl]benzonitrile is known for its potential as an intermediate or building block in various organic synthesis processes and pharmaceutical research.

Uses

Used in Organic Synthesis:
2-Fluoro-4-[(trans,trans)-4'-propyl[1,1'-bicyclohexyl]-4-yl]benzonitrile is utilized as a key intermediate in organic synthesis for the creation of more complex molecules. Its unique structure allows for the development of novel compounds with specific properties, making it a valuable component in the synthesis of advanced materials.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Fluoro-4-[(trans,trans)-4'-propyl[1,1'-bicyclohexyl]-4-yl]benzonitrile serves as a building block for the design and development of new drugs. Its incorporation into drug molecules can potentially enhance their efficacy, selectivity, and pharmacokinetic properties, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
2-Fluoro-4-[(trans,trans)-4'-propyl[1,1'-bicyclohexyl]-4-yl]benzonitrile is also employed in chemical research to study the effects of structural modifications on the properties and reactivity of molecules. This can lead to a better understanding of chemical behavior and the discovery of new reactions or applications.
While the specific applications and biological activities of 2-Fluoro-4-[(trans,trans)-4'-propyl[1,1'-bicyclohexyl]-4-yl]benzonitrile may vary depending on its interactions with other compounds or biological systems, its role in organic synthesis, pharmaceutical research, and chemical research highlights its importance in the development of new technologies and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 93743-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,4 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93743-04:
(7*9)+(6*3)+(5*7)+(4*4)+(3*3)+(2*0)+(1*4)=145
145 % 10 = 5
So 93743-04-5 is a valid CAS Registry Number.

93743-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-cyano-3-fluoro-1-[trans-4--(trans-4-propylcyclohexyl)-cyclohexyl]benzene

1.2 Other means of identification

Product number -
Other names 2-Fluoro-4-(4'-propyl-bicyclohexyl-4-yl)-benzonitrile

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:93743-04-5 SDS

93743-04-5Upstream product

93743-04-5Downstream Products

93743-04-5Relevant articles and documents

Process for the preparation of rod-like compounds

-

, (2008/06/13)

Compounds of the formula I, R1-(Ao)k-(Z1-A1)m-Zo-(E)n-(A2)o-(Z2-A3)p-R2 I, can be obtained from organoboron compounds of the formula II, R1-(Ao)k-(Z1-A1)m-Zo-B(Y)2 II, and compounds of the formula III, X-(E)n-(A2)o-(Z2-A3)p-R2 III, wherein is the compounds of the formulae I, II and III Ao, A1, A2, E, R1, R2, Zo, Q, X, Y, K, m, n, o and p have the meaning given in claim 1 by coupling in the presence of a metal compound in high yields.

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