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15732-69-1

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15732-69-1 Usage

Structure

Cyclic compound with a central ring of six carbon atoms and three selenium atoms attached

Substitution

Three methyl groups at the 2, 4, and 6 positions

Classification

Organoselenium compound

Potential properties

Antioxidant, antibacterial, and anticancer

Uses

Pharmaceutical, materials science, and industrial chemistry applications

Check Digit Verification of cas no

The CAS Registry Mumber 15732-69-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,3 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15732-69:
(7*1)+(6*5)+(5*7)+(4*3)+(3*2)+(2*6)+(1*9)=111
111 % 10 = 1
So 15732-69-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H12Se3/c1-4-7-5(2)9-6(3)8-4/h4-6H,1-3H3

15732-69-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-trimethyl-1,3,5-triselenane

1.2 Other means of identification

Product number -
Other names 2,4,6-Trimethyl-1,3,5-triselenan = Triselenoparaldehyd

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:15732-69-1 SDS

15732-69-1Downstream Products

15732-69-1Relevant articles and documents

Credali et al.

, p. 117 (1967)

NOVAL SYNTHESIS OF 1,3,5-TRISELENANES FROM ALDEHYDES, AND NOVEL GENERATION OF SELENOALDEHYDES BY FRAGMENTATION OF 1,3,5-TRISELENANES

Takikawa, Yuji,Uwano, Akira,Watanabe, Hiroyuki,Asanuma, Masaki,Shimada, Kazuaki

, p. 6047 - 6050 (2007/10/02)

Reaction of aldehydes with (Me3Si)2Se in the presence of Lewis acid afforded 1,3,5-triselenanes via selenoaldehydes.Novel and convenient generation of selenoaldehydes was also achived by thermally- or Lewia acid-induced fragmentation of 1,3,5-triselenanes.

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