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Benzene, 1-(1,3-butadienyl)-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62982-07-4

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62982-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62982-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,8 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62982-07:
(7*6)+(6*2)+(5*9)+(4*8)+(3*2)+(2*0)+(1*7)=144
144 % 10 = 4
So 62982-07-4 is a valid CAS Registry Number.

62982-07-4SDS

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 1-(3-methylphenyl)buta-1,3-diene

1.2 Other means of identification

Product number -
Other names 1-Buta-1,3-dien-ξ-yl-3-methyl-benzol

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:62982-07-4 SDS

62982-07-4Relevant academic research and scientific papers

Palladium-Catalyzed Synthesis of Indolines from Aroyloxycarbamates through a Tandem Decarboxylative Amination/Heck/Annulation Reaction

Wang, Zheng,Li, Peihe,Fu, Hui,Dai, Qipu,Hu, Changwen

, p. 192 - 200 (2018/11/23)

A novel synthesis of functionalized indolines via a Pd-catalyzed tandem decarboxylative amination/Heck/annulation reaction has been developed. This process features operational simplicity, mild conditions, and the use of a readily available and environmentally friendly starting material, namely carboxylic acid. Furthermore, the reaction shows good functional group tolerance and chemical selectivity. (Figure presented.).

Radical-Mediated Heck-Type Alkylation: Stereoconvergent Synthesis of Functionalized Polyenes

Zhang, Hong,Wu, Xinxin,Wei, Yunlong,Zhu, Chen

supporting information, p. 7568 - 7572 (2019/10/02)

The stereospecific synthesis of polyenes is of great synthetic value. Disclosed herein is a new, efficient, stereoconvergent approach for the synthesis of functionalized polyenes via a radical-mediated Heck-type alkylation. The easily accessed Z- and E-mixed alkenes are harnessed as starting material, leading to a unique stereoisomer of polyenes. In addition, the transformation features mild reaction conditions and broad functional group compatibility. A variety of valuable 1,3-dienes and 1,3,5-trienes are afforded in useful yields.

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