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65212-10-4

65212-10-4

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65212-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65212-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,1 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65212-10:
(7*6)+(6*5)+(5*2)+(4*1)+(3*2)+(2*1)+(1*0)=94
94 % 10 = 4
So 65212-10-4 is a valid CAS Registry Number.

65212-10-4SDS

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 Se-(4-chlorobenzoyl)selanyl 4-chlorobenzenecarboselenoate

1.2 Other means of identification

Product number -
Other names Bis-(4-chlorbenzoyl)diselenid

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:65212-10-4 SDS

65212-10-4Relevant articles and documents

Organoselenosilane-mediated selective mild access to selenolesters, selenoanhydrides and diacyl diselenides

Capperucci, Antonella,Deglinnocenti, Alessandro,Tiberi, Caterina

experimental part, p. 2248 - 2252 (2011/10/31)

Reaction of acyl chlorides with phenylselenotrimethyl-silane promoted by TBAF afforded a mild general access to selenolesters in good yields. When acyl chlorides were reacted with bis(trimethylsilyl)selenide (HMDSS) in 2:1 or 1:1 ratio a selective entry t

Synthesis of sodium diselenides and its reaction with benzoyl chloride under phase transfer catalysis and microwave irradiation conditions

Wang, Jin-Xian,Bai, Lin,Liu, Zhanxiang

, p. 971 - 977 (2007/10/03)

A simple, fast and efficient procedure for the synthesis of dibenzoyl diselenides involves the reaction of selenium with sodium hydroxide under phase transfer catalysis and microwave irradiation conditions to give sodium diselenides, which reacts with ben

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