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99766-23-1

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99766-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99766-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,7,6 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 99766-23:
(7*9)+(6*9)+(5*7)+(4*6)+(3*6)+(2*2)+(1*3)=201
201 % 10 = 1
So 99766-23-1 is a valid CAS Registry Number.

99766-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-bromophenyl)-2-[2-(4-bromophenyl)-2-oxoethyl]tellanylethanone

1.2 Other means of identification

Product number -
Other names -

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:99766-23-1 SDS

99766-23-1Relevant articles and documents

A new synthetic method for diphenacyl telluride Synthesis of some new organotellurium compounds containing Ar-COCH(R) groups via α-tellurocynatoketones

Al-Rubaie, Ali Z.,Yousif, Lina Z.,Al-Ba'aj, Ammar K.

, p. 40 - 46 (2007/10/03)

A new series of organotellurocyanate containing Ar-COCH(R) groups (i.e., C6H5COCH2TeCN (1), 4-BrC6H4COCH2TeCN 2), 4-PhC6H4COCH2TeCN (3) and C6H5COCH(CH3)TeCN (4)) were prepared by reacting KTeCN with the appropriate α-bromoketone in dry DMSO solution. Treatment of 1, 2, 3 and 4 with 10% NaOH afforded ditellurides 5, 6, 7 and 8 in high yields. Refluxing the ditelluride with activated copper powder in dry dioxane gave the corresponding tellurides (9, 10, 11 and 12) in good yields. Treatment of tellurides with thionyl chloride, bromine and iodine gave the dichloride (13-16), dibromide (17-20) and diiodide (21-24), respectively, in high yields. Both, tellurocyanate (1-4) and ditelluride (5-8) gave the trichloride (25-28), tribromide (29-32) and triiodide (33-36) when reacted with SOCl2, Br2 and I2, respectively. Treatment of 9-16 with m-chloroperbenzoic acid (MCPBA) afforded the corresponding alkyl aryl ketones in fair to good yields. All the compounds were characterized by elemental analysis and spectroscopic data.

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