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1-(4-Chlorophenyl)-1,3-cyclohexadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68099-22-9

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68099-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68099-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,9 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68099-22:
(7*6)+(6*8)+(5*0)+(4*9)+(3*9)+(2*2)+(1*2)=159
159 % 10 = 9
So 68099-22-9 is a valid CAS Registry Number.

68099-22-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Chlorophenyl)-1,3-cyclohexadiene

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:68099-22-9 SDS

68099-22-9Relevant academic research and scientific papers

Palladium-Catalyzed Asymmetric Tandem Denitrogenative Heck/Tsuji-Trost of Benzotriazoles with 1,3-Dienes

Li, Yin-Lin,Wu, Hai-Hong,Zhang, Junliang,Zhang, Pei-Chao

supporting information, p. 13010 - 13015 (2021/09/07)

The asymmetric denitrogenative cycloaddition has emerged as a powerful tool to build chiral aza-heterocyles. However, only one example of asymmetric denitrogenative cycloaddition of benzotriazole with unsaturated hydrocarbons has been explored so far, bec

Electrophilic cyanation of allylic boranes: Synthesis of β,γ-unsaturated nitriles containing allylic quaternary carbon centers

Kiyokawa, Kensuke,Hata, Shotaro,Kainuma, Shunpei,Minakata, Satoshi

supporting information, p. 458 - 461 (2019/01/10)

The electrophilic cyanation of allylic boranes, a process that is applicable to the construction of allylic quaternary carbon centers, is reported. The reaction has a broad substrate scope with a high functional group tolerance. The results represent an u

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