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Benzene, 1-[(1-ethenyl-3-butenyl)sulfonyl]-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85217-80-7

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85217-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85217-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,1 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85217-80:
(7*8)+(6*5)+(5*2)+(4*1)+(3*7)+(2*8)+(1*0)=137
137 % 10 = 7
So 85217-80-7 is a valid CAS Registry Number.

85217-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hexa-1,5-dien-3-ylsulfonyl-4-methylbenzene

1.2 Other means of identification

Product number -
Other names hexa-1,5-dien-3-yl p-tolyl sulphone

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:85217-80-7 SDS

85217-80-7Relevant academic research and scientific papers

Preparation of some Allylic Sulphones; Base-catalysed Isomerisation and Deuteriation of Cyclohex-2-enyl p-Tolyl Sulphones

Knight, Derek J.,Lin, Peter,Russell, Simon T.,Whitham, Gordon H.

, p. 2701 - 2706 (2007/10/02)

A summary of the methods used in the preparation of a range of allylic sulphones is given.In the case of the conformationally biased sulphones (5) and (6) stereospecific preparation from the cis- and trans-5-t-butylcyclohex-2-en-1-ols was achieved by rear

PALLADIUM-CATALYZED REACTION OF ALLYL CARBAMATES; ALLYLATION OF CARBONUCLEOPHILES, AND PROTECTION-DEPROTECTION OF AMINES

Minami, Ichiro,Ohashi, Yukihiro,Shimizu, Isao,Tsuji, Jiro

, p. 2449 - 2452 (2007/10/02)

Allylation of carbonucleophiles with allylic carbamates under neutral conditions has been studied.The C-allylation of carbonucleophile is competitive with the N-allylation of amines, and the structure of amines is crucial for the selectivity.Bulky secondary amines gave the best results.Also a new method of protection-deprotection of amines as carbamates has been developed.Smooth deprotection is possible by the palladium-catalyzed reaction of allyl carbamates with formic acid.This method is particulary useful for primary amines, including optically active amino acids.

Allylic Carbonates. Efficient Allylating Agents of Carbonucleophiles in Palladium-Catalyzed Reactions under Neutral Conditions

Tsuji, Jiro,Shimizu, Isao,Minami, Ichiro,Ohashi, Yukihiro,Sugiura, Teruo,Takahashi, Kazuhiko

, p. 1523 - 1529 (2007/10/02)

Allylation of β-keto esters or malonates was carried out in good yields under neutral conditions by using allylic carbonates in the presence of palladium-phospine catalyst.Although simple ketones, esters, nitriles, and sulfones hardly react with allylic carbonates, α-alkenyl or α-aryl ketones, esters, nitriles, and sulfones were also allylated by using palladium-bis(diphenylphosphino)ethane catalyst under neutral conditions.

FACILE PALLADIUM CATALYZED DECARBOXYLATIVE ALLYLATION OF ACTIVE METHYLENE COMPOUNDS UNDER NEUTRAL CONDITIONS USING ALLYLIC CARBONATES

Tsuji, Jiro,Shimizu, Isao,Minami, Ichiro,Ohashi, Yukihiro

, p. 4809 - 4812 (2007/10/02)

Palladium catalyzed decarboxylative allylation of active methylene compounds proceeded under mild neutral conditions using allylic carbonates, which are much more reactive than allylic acetates or phenoxides used commonly in the reaction.

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