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Benzenemethanol, a-[1-(phenyltelluro)ethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85698-67-5

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85698-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85698-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,9 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85698-67:
(7*8)+(6*5)+(5*6)+(4*9)+(3*8)+(2*6)+(1*7)=195
195 % 10 = 5
So 85698-67-5 is a valid CAS Registry Number.

85698-67-5SDS

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-Phenyl-2-(phenyltelluro)-2-propen-1-ol

1.2 Other means of identification

Product number -
Other names 1-phenyl-3-phenyltellurio-2-propen-1-ol

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:85698-67-5 SDS

85698-67-5Downstream Products

85698-67-5Relevant academic research and scientific papers

Indium(I) Iodide-Mediated Chemo-, Regio-, and Stereoselective Hydrotelluration of 2-Alkyn-1-ol Derivatives

Barros, Olga Soares do Rego,Lang, Ernesto Schulz,Peppe, Clovis,Zeni, Gilson

, p. 1725 - 1727 (2007/10/03)

Indium(I) iodide promotes the rigorous chemo-, regio-, and stereoselective hydrotelluration of 2-alkyn-1-ol derivatives with diphenylditelluride. The Markovnikov adducts with stereochemistry corresponding to an anti addition of the tellurol constituents a

New Reagents, XXVI. (Phenyltelluro)ethene, 1-Lithio-1-(phenyltelluro)ethene, and (Phenyltelluro)ethyne, Synthesis and Reactions

Kauffmann, Thomas,Ahlers, Holger

, p. 1001 - 1008 (2007/10/02)

(Phenyltelluro)ethene (2a, 78percent) and -ethyne (4, 51percent) were synthesized for the first time.By lithiation with bulky lithium amides (lithium 2,2,6,6-tetramethylpiperidide and lithium dicyclohexylamide) 1-lithio-1-(phenyltelluro)ethene (2b) was obtained from 2a (ca. 50percent yield). 2b reacts with benzaldehyde and chlorotrimethylsilane to give the expected products 2c (88percent) and 2e (80percent), respectively, but no reaction occurred with 1-iodopropane and allyl bromide.

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