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1-(propyltellanyl)propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64501-17-3

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64501-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64501-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,0 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64501-17:
(7*6)+(6*4)+(5*5)+(4*0)+(3*1)+(2*1)+(1*7)=103
103 % 10 = 3
So 64501-17-3 is a valid CAS Registry Number.

64501-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-propyltellanylpropane

1.2 Other means of identification

Product number -
Other names di-n-propyl telluride

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:64501-17-3 SDS

64501-17-3Downstream Products

64501-17-3Relevant academic research and scientific papers

NEW ROUTE TO ORGANIC SELENIDES AND TELLURIDES

Korchevin, N. A.,Podkuiko, P. A.,Stankevich, V. K.,Deryagina, E. N.,Trofimov, B. A.

, p. 85 - 87 (2007/10/03)

A new simple and convenient synthetic route to organic chalcogenides R2Y (R = alkyl, allyl, benzyl; Y = Se, Te) is developed, which involves generation of Se2- and Te2- anions from Se and Te in the system KOH-hydrazine hydrate, where the latter plays the role of both the medium and reducing agent.Subsequent alkylation of the anions with the corresponding alkyl halides furnishes the target chalcogenides in almost 95percent yield.Alkyl chlorides react faster than alkyl bromides and alkyl iodides.

A New Route for the Synthesis of Dialkyl Tellurides and Dialkyl Ditellurides

Bhasin, K.K.,Gupta, Vijay,Gautam, A.,Sharma, R.P.

, p. 2191 - 2195 (2007/10/02)

Sodium cleaves elemental tellurium, Tex, quantitatively to Te2-2 and Te2- in anhydrous tetrahydrofuran in the presence of catalytic amounts of naphthalene.Subsequent addition of alkylating agent affords dialkyl tellurides and dialkyl ditellurides in excellent yields.

ALKYLVINYL TELLURIDES FROM TELLURIUM, ACETYLENE AND ALKYL HALIDES

Trofimov, B. A.,Gusarova, N. K.,Tatarinova, A. A.,Potapov, V. A.,Sinegovskaya, L. M.,et. al.

, p. 6739 - 6744 (2007/10/02)

Synthetic routes to alkylvinyl tellurides by direct reaction of metallic tellurium, acetylene and alkyl halide in the system KOH-SnCl2-H2O and successive interaction of divinyl telluride with lithium and alkyl halide in liquid ammonia have been developed.

REACTIONS OF CHALCOGENS WITH ACETYLENES. ALKYL VINYL TELLURIDES FROM TELLURIUM, ACETYLENE, AND ALKYL HALIDES

Gusarova, N. K.,Trofimov, B. A.,Tatarinova, A. A.,Potapov, V. A.,Sinegovskaya, L. M.,at al.

, p. 1686 - 1691 (2007/10/02)

Methods were developed for the synthesis of alkyl vinyl tellurides from metallic tellurium, acetylene, and alkyl halides in the KOH-SnCl2-H2O system and also by the successive action of lithium and alkyl halide on divinyl telluride in liquid ammonia.

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