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4-(3,5-DIMETHYLPHENYL)-1-BUTENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77446-28-7

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77446-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77446-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,4 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77446-28:
(7*7)+(6*7)+(5*4)+(4*4)+(3*6)+(2*2)+(1*8)=157
157 % 10 = 7
So 77446-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H16/c1-4-5-6-12-8-10(2)7-11(3)9-12/h4,7-9H,1,5-6H2,2-3H3

77446-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-but-3-enyl-3,5-dimethylbenzene

1.2 Other means of identification

Product number -
Other names 4-(3,5-DIMETHYLPHENYL)-1-BUTENE

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:77446-28-7 SDS

77446-28-7Downstream Products

77446-28-7Relevant academic research and scientific papers

Designed electron-deficient gold nanoparticles for a room-temperature Csp3-Csp3coupling reaction

Yu, Qiu-Ying,Su, Hui,Zhai, Guang-Yao,Zhang, Shi-Nan,Sun, Lu-Han,Chen, Jie-Sheng,Li, Xin-Hao

, p. 741 - 744 (2021)

Stille cross-coupling reactions catalysed by an ideal catalyst combining the high activity of homogeneous catalysts and the reusability of heterogeneous catalysts are of great interest for C-C bond formation, which is a widely used reaction in fine chemistry. Despite great effort to increase the utilization ratio of surface metal atoms, the activity of heterogeneous catalysts under mild conditions remains unsatisfactory. Herein, we design a proof-of-concept strategy to trigger the room-temperature activity of heterogeneous Au catalysts by decreasing the electron density at the interface of a rationally designed Schottky heterojunction of Au metals and boron-doped carbons. The electron-deficient Au nanoparticles formed as a result of the rectifying contact with boron-doped carbons facilitate the autocleavage of C-Br bonds for highly efficient C-C coupling reactions of alkylbromides and allylstannanes with a TOF value of 5199 h-1 at room temperature, surpassing that of the state-of-the-art homogeneous catalyst. This journal is

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