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Benzene, 1-[[1-ethenyl-1-(2-propenyl)-3-butenyl]sulfonyl]-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84603-00-9

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84603-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84603-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,0 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84603-00:
(7*8)+(6*4)+(5*6)+(4*0)+(3*3)+(2*0)+(1*0)=119
119 % 10 = 9
So 84603-00-9 is a valid CAS Registry Number.

84603-00-9SDS

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 4-(p-tolylsulphonyl)-4-vinyl-1,6-heptadiene

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:84603-00-9 SDS

84603-00-9Downstream Products

84603-00-9Relevant academic research and scientific papers

Phase transfer catalysis (ptc): a convenient tool for generation and reactions of allyl sulphonyl carbanions

Jonczyk, Andrzej,Radwan-Pytlewski, Tadeusz

, p. 111 - 119 (2007/10/03)

Allyl sulphones la-d or le react with alkyl halides (RX) in the presence of concentrated aqueous NaOH solution and tetrabutylammonium bromide (TBAB) as a catalyst to give, with high yields, mono(2a-d) or di-alkylated (3e) products, respectively. Under the same conditions sulphone If forms mixtures of the products, the composition of which depends on the structure of RX and the RX:lf ratio. With a,cu-dibromo alkanes, sulphones la,d-f give rise to cyclic products (7a,d-f) with low to excellent yields. With 4-nitrofluorobenzene (in solid NaOH-DMSO system) or vinyl acetate (by PTC) sulphone la affords the products 2al3 and 9a, respectively.

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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