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

501325-59-3

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501325-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501325-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,3,2 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 501325-59:
(8*5)+(7*0)+(6*1)+(5*3)+(4*2)+(3*5)+(2*5)+(1*9)=103
103 % 10 = 3
So 501325-59-3 is a valid CAS Registry Number.

501325-59-3SDS

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 p-bromobenzyl allyl sulfone

1.2 Other means of identification

Product number -
Other names Allyl-(4-brom-benzyl)-sulfon

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:501325-59-3 SDS

501325-59-3Upstream product

501325-59-3Relevant articles and documents

Synthesis of allyl sulfones from potassium allyltrifluoroborates

Stikute, Agnese,Lugi?ina, Jevge?ija,Turks, Māris

, p. 2727 - 2731 (2017)

Potassium allyltrifluoroborates underwent a bora-ene reaction with sulfur dioxide in the absence of Lewis acid catalysts to give sulfinyloxy-trifluoroborates, which subsequently undergo alkylation with electrophiles to produce sulfones in up to 91% yield. Benzyl halides and haloacetic acid derivatives can be used as the alkylation reagents while the Sanger reagent undergoes a SNAr reaction with sulfinyloxy-trifluoroborates to produce the corresponding 2,4-dinitrophenylsulfone. The developed method allows the transformation of potassium allyltrifluoroborates into allyl sulfones.

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