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1229-73-8

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1229-73-8 Usage

Appearance

Colorless, crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

a. Building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals
b. Manufacturing of optical brighteners, dyes, and plasticizers

Optical properties

Exhibits strong fluorescence

Sensitivity

Sensitive to light

Applications

a. Fluorescence spectroscopy
b. Photoresponsive material in photolithography applications

Biological activities

Studied for antifungal and photocytotoxic properties

Check Digit Verification of cas no

The CAS Registry Mumber 1229-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1229-73:
(6*1)+(5*2)+(4*2)+(3*9)+(2*7)+(1*3)=68
68 % 10 = 8
So 1229-73-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H15Cl/c21-19-13-11-16(12-14-19)15-20(17-7-3-1-4-8-17)18-9-5-2-6-10-18/h1-15H

1229-73-8SDS

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-chloro-4-(2,2-diphenylethenyl)benzene

1.2 Other means of identification

Product number -
Other names 2-(4-chloro-phenyl)-1,1-diphenyl-ethene

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:1229-73-8 SDS

1229-73-8Relevant articles and documents

Sequential reactions of trimethylstannyl anions with vinyl chlorides and dichlorides by the SRN1 mechanism followed by palladium-catalyzed cross-coupling processes

Corsico, Eduardo F.,Rossi, Roberto A.

, p. 6427 - 6432 (2004)

The reactions of trimethylstannyl ions (Me3Sn-) with vinyl chlorides in liquid ammonia give good yields of vinylstannanes. Some of them react in the dark, and others need light stimulation to react. The fact that these reactions are inhibited by radical and radical anion traps shows that they occur by the SRN1 mechanism. When the reaction takes place with 1,1-dichloro-1-alkenes, monosubstitution reduced products are formed in an E/Z mixture. The efficient synthesis of triarylolefins by Pd(0)-catalyzed cross-coupling reactions of vinylstannanes with several iodoarenes is reported. Similar yields were obtained in one-pot-type reactions.

Immobilized Pd on Eggshell Membrane: A powerful and recyclable catalyst for Suzuki and Heck cross-coupling reactions in water

Wu, Shang,Jiang, Hongyan,Zhang, Hong,Zhao, Lianbiao,Yuan, Peilin,Zhang, Ying,Su, Qiong,Wang, Yanbin,Wu, Lan,Yang, Quanlu

, (2020/09/09)

A stable heterogeneous palladium catalysts, the waste eggshell membrane (ESM) anchored Pd complex, was synthesized by a simple and green technique. The catalyst obtained can display an outstanding catalytic activity for Suzuki and Heck coupling reactions in water media. The reactions of various aryl halides with aryl boronic acids and terminal alkenes provided the corresponding products in moderate to excellent yields. More importantly, this novel and efficient catalyst with high stability can be easily reused for at least twelve times with no decrease of the catalytic activity, performing an endurable and wide tolerance of the substrates. Facile synthesis, high catalytic activity, and recyclability make these catalysts interesting for further studies.

Polysubstituted ethylene compound as well as preparation method and application thereof

-

Paragraph 0125-0129; 0245-0249, (2020/12/30)

The invention discloses a polysubstituted ethylene compound as well as a preparation method and application thereof. The invention particularly discloses a preparation method of a polysubstituted ethylene compound as shown in a formula III, which comprises the following step: in an organic solvent, carrying out reaction as shown in the specification on a compound as shown in a formula I and a compound as shown in a formula II in the presence of a palladium catalyst, a phosphine ligand and alkali to obtain the polysubstituted ethylene compound as shown in the formula III. The preparation methodcan be suitable for various types of substrates, and the configuration of double bonds is controllable.

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