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Benzenesulfonamide, N-(di-2-furanylmethyl)-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

488720-06-5

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488720-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 488720-06-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,8,7,2 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 488720-06:
(8*4)+(7*8)+(6*8)+(5*7)+(4*2)+(3*0)+(2*0)+(1*6)=185
185 % 10 = 5
So 488720-06-5 is a valid CAS Registry Number.

488720-06-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[bis(furan-2-yl)methyl]-4-methylbenzenesulfonamide

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:488720-06-5 SDS

488720-06-5Downstream Products

488720-06-5Relevant academic research and scientific papers

Synthesis of 3-sulfonyloxypyridines: Oxidative ring expansion of α-furyl-sulfonamides and N→O sulfonyl transfer

Hodgson, Robert,Kennedy, Andrew,Nelson, Adam,Perry, Alexis

, p. 1043 - 1046 (2008/02/13)

N-Sulfonyl pyridinones derived from α-furylsulfonamides may be aromatised with concomitant N→O sulfonyl transfer to produce 3-sulfonyloxypyridines. Georg Thieme Verlag Stuttgart.

Desymmetrisation of meso difuryl alcohols, diols and their derivatives: Complementary directed and undirected asymmetric dihydroxylation reactions

Hodgson, Robert,Majid, Tahir,Nelson, Adam

, p. 1631 - 1643 (2007/10/03)

Asymmetric reactions (for example, asymmetric epoxidation and asymmetric dihydroxylation) were examined for the desymmetrisation of the meso substrates 1,1-difuran-2-ylmethanol,N-(1,1-difuran-2-ylmethyl)-4- methylbenzenesulfonamide, (R,S)-1,4-difuran-2-yl

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