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128496-94-6

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128496-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128496-94-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,4,9 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128496-94:
(8*1)+(7*2)+(6*8)+(5*4)+(4*9)+(3*6)+(2*9)+(1*4)=166
166 % 10 = 6
So 128496-94-6 is a valid CAS Registry Number.

128496-94-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2,3-Dibromo-1-(phenylsulfonyl)-1-propene

1.2 Other means of identification

Product number -
Other names E-2,3-dibromo-1-(phenylsulfonyl)-1-propene

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:128496-94-6 SDS

128496-94-6Relevant articles and documents

Improved synthesis of 2,3-dibromo-1-(phenylsulfonyl)-1-propene (DBP)

VanZanten, Aaron,Mullaugh, Katherine,Harrington, Ryan,Kiefer, Adam,Carlson, David,Mastarone, Dan,Lipchik, Corey,Murphree, S. Shaun

, p. 2611 - 2613 (2004)

A convenient preparation of 2,3-dibromo-1-(phenylsulfonyl)-1-propene (DBP, 1) is available through the one-pot propargylation and oxidation of thiophenol to give the propargyl sulfone 11, which is isomerized and brominated in another one-pot reaction. The

Tunable Regioselectivity Associated with the Reaction of 2,3-Dihalo-1-(phenylsulfonyl)-1-propenes with Ambident Nucleophilic Reagents

Padwa, Albert,Austin, David J.,Ishida, Masaru,Muller, Cheryl L.,Murphree, S. Shaun,Yeske, Philip E.

, p. 1161 - 1169 (2007/10/02)

2,3-Dihalo-1-(phenylsulfonyl)-1-propenes, obtained by the addition of bromine or iodine onto (phenylsulfonyl)propadiene, were found to exhibit interesting reactivity as both mono- and dielectrophiles, with the mode of reactivity depending upon the nature

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