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2-Cyclopenten-1-ol, 4-(1,3,3-triphenyl-1,2-propadienyl)-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86296-80-2

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86296-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86296-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,9 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86296-80:
(7*8)+(6*6)+(5*2)+(4*9)+(3*6)+(2*8)+(1*0)=172
172 % 10 = 2
So 86296-80-2 is a valid CAS Registry Number.

86296-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,4S)-4-(1,3,3-triphenylpropa-1,2-dienyl)cyclopent-2-en-1-ol

1.2 Other means of identification

Product number -
Other names -

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:86296-80-2 SDS

86296-80-2Downstream Products

86296-80-2Relevant academic research and scientific papers

Silver Trifluoroacetate Initiated Reactions of Chlorotriphenylallene with Cyclopentadiene - Vinyl Cation Type Cycloadditions of Allenyl Cations

Baeuml, Englbert,Mayr, Herbert

, p. 683 - 693 (2007/10/02)

Chlorotriphenylallene (8) and cyclopentadiene react in the presence of equimolar amounts of silver trifluoroacetate to give a mixture of trifluoroacetates which hydrolyse to the alcohols 16 - 21.The intermediate triphenylallenyl cation (9) is exclusively

CONCERTED AND STEPWISE CYCLOADDITIONS OF THE TRIPHENYLALLENYL CATION WITH CYCLOPENTADIENE

Mayr, Herbert,Baeuml, Englbert

, p. 357 - 360 (2007/10/02)

The triphenylallenyl cation (5), generated in situ under different conditions, reacts with cyclopentadiene via allyl cations 7 and 9.The exclusive formation of 7 from 12 and FSO3H proves a concerted cycloaddition leading to 9 and suggests a stepwise cycloaddition reaction to give 7.

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