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40941-17-1

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40941-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40941-17-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,4 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40941-17:
(7*4)+(6*0)+(5*9)+(4*4)+(3*1)+(2*1)+(1*7)=101
101 % 10 = 1
So 40941-17-1 is a valid CAS Registry Number.

40941-17-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzenesulfonylmethyl)-5-nitrofuran

1.2 Other means of identification

Product number -
Other names 5-nitrofurfuryl phenyl sulfone

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:40941-17-1 SDS

40941-17-1Downstream Products

40941-17-1Relevant articles and documents

PREPARATION AND ALKYLATION REACTIONS OF 4-NITROBENZYL AND 5-NITROFURFURYL SULFONES

Prousek, Josef

, p. 851 - 856 (2007/10/02)

Substitution reaction of 5-nitrofurfuryl bromide (I) with sodium thiophenoxide and 4-chlorothiophenoxide in dimethyl sulfoxide at 20 deg C and oxidation with dimethyl sulfoxide in the reaction medium afforded 5-nitrofurfuryl phenyl sulfone (IVa) and 5-nit

ELECTRON TRANSFER PROCESSES. REACTION OF 5-NITROFURYL DERIVATIVES GOING BY ANIONRADICAL MECHANISM

Prousek, Josef

, p. 3347 - 3353 (2007/10/02)

5-nitrofurfuryl nitrate and bromide (1a,b) react with electron donors to give 1,2-bis(5-nitro-2-furyl)ethane (II), 1,2-bis(5-nitro-2-furyl)ethylene (III), 5-nitro-2-methylfurane (IV), products of SRN1 reactions Va, Vb and other derivatives.Formation of the derivatives II to V is discussed on the basis of anionradical mechanism. 5-Nitrobenzyl bromide reacts by a SRN1 reaction with 5-nitrofurfuryl phenyl sulphone (Va) in basic medium to give 1-(5-nitro-2-furyl)-1-phenylsulphonyl-2-(4-nitrophenyl)ethane (VIII) and 1-(5-nitro-2-furyl)-2-(4-nitrophenyl)ethylene (IX).

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