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189516-38-9

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189516-38-9 Usage

Molecular weight

304.51 g/mol

Chemical family

Furanones

Structure

Dihydrofuranone derivative

Tris(1-methylethyl)silyl group

A group consisting of three (CH3)3Sigroups attached to an oxygen atom.

Chirality

The compound has a stereocenter at the 5-position, designated as (5S).

Uses

Fragrance ingredient in perfumes, building block in the synthesis of other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 189516-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,5,1 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 189516-38:
(8*1)+(7*8)+(6*9)+(5*5)+(4*1)+(3*6)+(2*3)+(1*8)=179
179 % 10 = 9
So 189516-38-9 is a valid CAS Registry Number.

189516-38-9SDS

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 (5S)-5-[tri(propan-2-yl)silyloxymethyl]oxolan-2-one

1.2 Other means of identification

Product number -
Other names -

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:189516-38-9 SDS

189516-38-9Relevant articles and documents

Study of butyrolactones related to sub-type 3 annonaceous acetogenins. Structure revision of itrabiu, jetein, laherradurin and otivarin

Warmerdam, Erwin,Tranoy, Isabelle,Renoux, Brigitte,Gesson, Jean-Pierre

, p. 8077 - 8080 (1998)

Starting from 5(S)-hydroxymethyl-γ-butyrolactone 1, lactones related to title acetogenins have been prepared in few steps. This study leads to a structure revision of the lactone configurations of these acetogenins.

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