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138767-59-6

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138767-59-6 Usage

Type of compound

Heterocyclic compound

Elements present

Carbon (C), Hydrogen (H), Nitrogen (N), Sulfur (S), and Silicon (Si)

Structure

Contains a silicon atom, nitrogen atoms, and a sulphur atom

Functional groups

Triazine ring, methyl groups, and phenyl groups

Reactivity

Reactive intermediate used in organic synthesis

Applications

Pharmaceutical and agrochemical industries, material science, and catalysis

Unique properties

Valuable tool for the development of new chemical processes and materials due to its unique structure and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 138767-59-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,6 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138767-59:
(8*1)+(7*3)+(6*8)+(5*7)+(4*6)+(3*7)+(2*5)+(1*9)=176
176 % 10 = 6
So 138767-59-6 is a valid CAS Registry Number.

138767-59-6SDS

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 1,2,5-trimethyl-2,3-diphenyl-1,3,5,2-triazasilepane-4-thione

1.2 Other means of identification

Product number -
Other names 1,3,5-Triaza-2-silacycloheptane-4-thione,1,2,5-trimethyl-2,3-diphenyl

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:138767-59-6 SDS

138767-59-6Relevant articles and documents

Aminosilylation of heterocumulenes and the intramolecular decomposition of their silyl-functionalized adducts

Corriu, R. J. P.,Lanneau, Gerard F.,Mehta, V. D.

, p. 9 - 26 (2007/10/02)

Heteroorganic amidosilanes are readily obtained by interaction of CO2, CS2 and other heterocumulenes with pentacoordinated diaminosilanes.A comparison is made with the corresponding reactions of tetracoordinated species.Decompositon of these bifunctional organosilanes gives 2-substituted ureido derivatives and base-stabilized low coordinated silicon species, seemingly by a unimolecular thermal β-elimination.

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