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Benzene, 1-(chlorotellurinyl)-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77443-67-5

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77443-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77443-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,4 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77443-67:
(7*7)+(6*7)+(5*4)+(4*4)+(3*3)+(2*6)+(1*7)=155
155 % 10 = 5
So 77443-67-5 is a valid CAS Registry Number.

77443-67-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chlorotellurinyl-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names 4-Methoxyphenyltellurium oxochloride

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:77443-67-5 SDS

77443-67-5Relevant articles and documents

SYNTHESIS AND STRUCTURES OF AROMATIC AND HETEROCYCLIC TELLURIUM COMPOUNDS. XXXI. REACTIONS OF ARYLTELLURIUM OXOCHLORIDES

Rivkin, B. B.,Maksimenko, A. A.,Sadekov, I. D.

, p. 1049 - 1055 (2007/10/02)

The reactions of aryltellurium oxochlorides with the lowest aliphatic acid anhydrides lead to diaryltellurium dichlorides, Te, and CO2 through the intermediate formation of diaryltellurium chloride diacylates.Aryltellurium trichlorides and carboxylic acid anhydrides are formed in the reaction with acyl chlorides.The chlorine atom in the tellurium oxochlorides is replaced by a phenyl group on reaction with phenyllithium.The reaction with dimedone in the presence of triethylamine leads to diaryl ditellurides and a product of trimerization of a carbene, viz., a dimedone derivative that is formed in the thermal decomposition of the intermediate ylid.

COMPOUNDS WITH A TELLURIUM-NITROGEN BOND. N-(ARYLSULFONYL)ARENETELLURINIMIDOYL HALIDES

Stukalo, E. A.,Kisilenko, A. A.,Markovskii, L. N.

, p. 2184 - 2188 (2007/10/02)

In the reaction of diaryl ditellurides and aryltellurenyl chlorides with N,N-dihalogenoarenesulfonamides N-(arylsulfonyl)arenetellurinimidoyl halides are formed.The same compounds are obtained in the reaction of aryltellurium trihalides with disilylated arenesulfonamides.The reactions of the acid halides with trimethylsilylmorpholine leads to the formation of the morpholides of N-(arylsulfonyl)arenetellurinimidic acids, and the reaction with hydrogen chloride, water, and dimedone is accompanied by cleavage of the tellurium-nitrogen bond with the formation of aryltellurium trihalides, arenetellurinyl halides, and telluronium ylides.

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