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dimethyl 2-selenoxo-1,3-diselenole-4,5-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57653-12-0

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57653-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57653-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,5 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57653-12:
(7*5)+(6*7)+(5*6)+(4*5)+(3*3)+(2*1)+(1*2)=140
140 % 10 = 0
So 57653-12-0 is a valid CAS Registry Number.

57653-12-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-selanylidene-1,3-diselenole-4,5-dicarboxylate

1.2 Other means of identification

Product number -
Other names 4,5-Dicarbomethoxy-1,3-diselenol-2-selon

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:57653-12-0 SDS

57653-12-0Downstream Products

57653-12-0Relevant academic research and scientific papers

Synthesis and downstream reactions of 2-(triphenylphosphino)-4,5-dicarbomethoxy-1,3-diselenole tetrafluoroborate: X-ray crystal structure of a nitroso derivative of a 2-ylidene-1,3-diselenole stabilized by an intramolecular O...Se interaction

Chesney, Antony,Bryce, Martin R.,Chalton, Michael A.,Batsanov, Andrei S.,Howard, Judith A. K.,Fabre, Jean-Marc,Binet, Laurent,Chakroune, Said

, p. 2877 - 2881 (1996)

The title 1,3-diselenole Wittig reagent 9 has been synthesised by a new, efficient route from readily-available starting materials and reacted with a variety of functionalized aldehydes to form the corresponding 2-ylidene-1,3-diselenones 12 in respectable yields. X-ray analysis of a nitrosated derivative 14e, prepared by the reaction of 12e with isoamyl nitrite, has provided the first direct evidence for the stabilization of such systems by intramolecular oxygen-selenium interactions.

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