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Benzenesulfonamide, 4-methyl-N-(9-phenyl-9H-selenoxanthen-9-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82238-29-7

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82238-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82238-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,3 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82238-29:
(7*8)+(6*2)+(5*2)+(4*3)+(3*8)+(2*2)+(1*9)=127
127 % 10 = 7
So 82238-29-7 is a valid CAS Registry Number.

82238-29-7SDS

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 4-methyl-N-(9-phenylselenoxanthen-9-yl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names 9-phenyl-9-(N-p-toluenesulfonamido)selenoxanthene

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:82238-29-7 SDS

82238-29-7Downstream Products

82238-29-7Relevant academic research and scientific papers

CHEMISTRY OF CIS- AND TRANS-9-PHENYLSELENOXANTHENE-N-ARYLSULFONYLSELENILIMINES

Tomimatsu, Kiminori,Kataoka, Tadashi,Shimizu, Hiroshi,Hori, Mikio

, p. 97 - 110 (2007/10/02)

cis- and trans-9-Phenylselenoxanthene-N-(arylsulfonyl)selenilimines were synthesized and isolated.Their stereochemistry was ascertained from the NMR spectra.Cis isomers reacted with chloramine-T or -B by an SN2 type substitution to form trans i

STEREOISOMERS OF SELENILIMINES: ISOLATION AND REACTIONS OF 9-PHENYLSELENOXANTHENE-N-ARYLSULFONYLSELENILIMINES

Hori, Mikio,Kataoka, Tadashi,Shimizu, Hiroshi,Tomimatsu, Kiminori

, p. 901 - 904 (2007/10/02)

The isolated cis- and trans-9-phenylselenoxanthene-N-arylsulfonylselenilimines were not interconverted thermally. cis-Isomers were converted to trans-isomers by chloramine-T or -B in a fashion of SN2 type substitution. cis-Isomers did not rearrange but trans-isomers rearranged thermally to 9-arylsulfonamido-9-phenylselenoxanthenes, whereas both isomers underwent the base-catalyzed intermolecular rearrangement.

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