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14255-64-2

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14255-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14255-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,5 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14255-64:
(7*1)+(6*4)+(5*2)+(4*5)+(3*5)+(2*6)+(1*4)=92
92 % 10 = 2
So 14255-64-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14/c1-2-4-6-8-9-7-5-3-1/h1-2,7,9H,3-6,8H2/b2-1-,9-7-

14255-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1Z,5Z)-cyclonona-1,5-diene

1.2 Other means of identification

Product number -
Other names cis,cis-cyclonona-1,5-diene

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:14255-64-2 SDS

14255-64-2Relevant articles and documents

Anet,Yavari

, p. 6496,6497 (1977)

Devaprabhakara,Gardner

, p. 648 (1963)

Devaprabhakara et al.

, p. 1553 (1963)

Annelations with Tetrachlorothiophene 1,1-Dioxide

Raasch, Maynard S.

, p. 856 - 867 (2007/10/02)

Tetrachlorothiophene 1,1-dioxide is a reactive, cheletropic Diels-Alder reagent.It has been used to annelate, with loss of sulfur dioxide, a large variety of olefinic compounds to form 1,2,3,4-tetrachloro-1,3-cyclohexadiene derivatives.Dehydrochlorination of these forms 1,2,4-trichloro aromatic compounds.Both double bonds in thiophene and N-methylpyrrole are annelated.Addition of tetrachlorothiophene dioxide to acyclic 1,5-dienes, which may contain a heteroatom, provides a facile synthesis of tetrachloroisotwistenes (51) and heteroisotwistenes (56) by a double Diels-Alder reaction.Acyclic 1,6-dienes lead to tetrachlorohomoisotwistene (59) and heterohomoisotwistenes (61).By use of 1,5-cyclooctadiene, sym-dibenzocyclooctatetraene, and 1,5-cyclononadiene, the more complex carbocycles 62, 65, and 66 are generated.Tetrabromothiophene dioxide reacts like the tetrachloro compound.

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