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Furan, 2-nitro-5-[(phenylthio)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40941-14-8

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40941-14-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40941-14-8 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 40941-14:
(7*4)+(6*0)+(5*9)+(4*4)+(3*1)+(2*1)+(1*4)=98
98 % 10 = 8
So 40941-14-8 is a valid CAS Registry Number.

40941-14-8SDS

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-nitro-5-(phenylsulfanylmethyl)furan

1.2 Other means of identification

Product number -
Other names Furan,2-nitro-5-[(phenylthio)methyl]

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:40941-14-8 SDS

40941-14-8Downstream Products

40941-14-8Relevant academic research and scientific papers

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

REACTION OF NUCLEOPHILES WITH ELECTRON ACCEPTORS BY SN2 OR SINGLE ELECTRON TRANSFER (S.E.T.) MECHANISMS: THIOLATES AND 2-HALOMETHYL-5-NITROFURANS.

Beadle, Charles D.,Bowman, W. Russell,Prousek, Josef

, p. 4979 - 4982 (2007/10/02)

Thiolates react with 2-halomethyl-5-nitrofurans to yield 5-nitrofurfuryl sulphides by a SN2(C) mechanism, and disulphides and 2-methyl-5-nitrofuran by a SN2(X) mechanism.

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