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5467-43-6

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5467-43-6 Usage

Type of compound

Polyphenyl compound

Structure

Three benzene rings linked together by a propynyl group

Propynyl group

Chain of three carbon atoms and a carbon-carbon triple bond

Applications

Organic synthesis, pharmaceuticals, dyes, and other organic compounds

Properties

Fluorescent

Uses

Development of fluorescent dyes and materials

Potential applications

Organic electronics and optoelectronics due to unique chemical structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 5467-43-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5467-43:
(6*5)+(5*4)+(4*6)+(3*7)+(2*4)+(1*3)=106
106 % 10 = 6
So 5467-43-6 is a valid CAS Registry Number.

5467-43-6SDS

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-diphenylprop-2-ynylbenzene

1.2 Other means of identification

Product number -
Other names 1',3',3'-trimethylspiro-<2H-1-benzopyran-2,2'-indoline>

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:5467-43-6 SDS

5467-43-6Relevant articles and documents

Site-Selective Csp3-Csp/Csp3-Csp2Cross-Coupling Reactions Using Frustrated Lewis Pairs

Dasgupta, Ayan,Stefkova, Katarina,Babaahmadi, Rasool,Yates, Brian F.,Buurma, Niklaas J.,Ariafard, Alireza,Richards, Emma,Melen, Rebecca L.

supporting information, p. 4451 - 4464 (2021/04/07)

The donor-acceptor ability of frustrated Lewis pairs (FLPs) has led to widespread applications in organic synthesis. Single electron transfer from a donor Lewis base to an acceptor Lewis acid can generate a frustrated radical pair (FRP) depending on the s

SeCl2-Mediated Approach Toward Indole-Containing Polysubstituted Selenophenes

Martins, Guilherme M.,Back, Davi F.,Kaufman, Teodoro S.,Silveira, Claudio C.

, p. 3252 - 3264 (2018/03/25)

A novel and efficient SeCl2-mediated chalcogenative cyclization strategy toward 3-selenophen-3-yl-1H-indoles from readily available and conveniently substituted propargyl indoles is described. It entails an unprecedented selenirenium-induced 1,

Cleavage of C–C and C–O Bonds to Form C–C Bonds: Direct Cross-Coupling between Acetylenic Alcohols and Benzylic Carbonates

Mi, Zhiyuan,Tang, Jiahao,Guan, Zhipeng,Shi, Wei,Chen, Hao

, p. 4479 - 4482 (2018/09/10)

A palladium-catalyzed cross-coupling reaction between C(sp) and C(sp3) centers was achieved in excellent yields via C–C bond cleavage and C–O bond cleavage. This procedure uses relatively stable acetylenic alcohols as reactants instead of unsta

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