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1483-68-7

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1483-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1483-68-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1483-68:
(6*1)+(5*4)+(4*8)+(3*3)+(2*6)+(1*8)=87
87 % 10 = 7
So 1483-68-7 is a valid CAS Registry Number.

1483-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,4-triphenylbuta-1,2,3-trienylbenzene

1.2 Other means of identification

Product number -
Other names Tetraphenylbutatriene

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:1483-68-7 SDS

1483-68-7Relevant articles and documents

Desulphurisation-Dimerisation of Dithioacetals with W(CO)6

Yeung, Lam Lung,Yip, Yu Chi,Luh, Tien-Yau

, p. 981 - 983 (1987)

Dithioacetals undergo desulphurisation-dimerisation to give the corresponding dimeric alkenes in good to excellent yields on treatment with W(CO)6.

Mechanosynthesis of Odd-Numbered Tetraaryl[n]cumulenes

Ardila-Fierro, Karen J.,Bolm, Carsten,Hernández, José G.

, p. 12945 - 12949 (2019/08/01)

A mechanochemical synthesis of one-dimensional carbon allotrope carbyne model compounds, namely tetraaryl[n]cumulenes (n=3, 5) was realized. Central for the mechanosynthesis of the cumulenic carbon nanostructures were the development of a mechanochemical Favorskii alkynylation-type reaction and the implementation of a solvent-free, acid-free reductive elimination with tin(II) chloride by ball milling.

Synthesis of cyano-substituted diaryltetracenes from tetraaryl[3]cumulenes

Gawel, Przemyslaw,Dengiz, Cagatay,Finke, Aaron D.,Trapp, Nils,Boudon, Corinne,Gisselbrecht, Jean-Paul,Diederich, Francois

, p. 4341 - 4345 (2014/05/06)

A versatile, two-step synthesis of highly substituted, cyano-functionalized diaryltetracenes has been developed, starting from easily accessible tetraaryl[3]cumulenes. This unprecedented transformation is initiated by [2+2] cycloaddition of tetracyanoethy

Palladium-catalyzed arylation of butadiynes

Dyker,Borowski,Henkel,Kellner,Dix,Jones

, p. 8259 - 8262 (2007/10/03)

Diarylbutadiynes 1 undergo a palladium-catalyzed coupling reaction with aryl halides 2 to give tetraarylbutatrienes 3, which may further react to benzofulvenes 6 depending on the reaction temperature and the type of aryl groups. (C) 2000 Elsevier Science

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