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1,3-Dioxolan-2-one, 4-methyl-5-methylene-4-(2-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

632291-67-9

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632291-67-9 Usage

Physical state

Colorless liquid

Odor

Strong, sweet

Industries

Pharmaceutical and fragrance industries

Use as a starting material

Synthesis of various compounds

Application in food products

Flavoring ingredient

Application in personal care products

Fragrance additive

Potential applications

Organic synthesis and preparation of bioactive compounds

Structure

Contains a 1,3-dioxolan-2-one ring, a 4-methyl group, a 5-methylene group, and a 2-phenylethyl group.

Check Digit Verification of cas no

The CAS Registry Mumber 632291-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,2,2,9 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 632291-67:
(8*6)+(7*3)+(6*2)+(5*2)+(4*9)+(3*1)+(2*6)+(1*7)=149
149 % 10 = 9
So 632291-67-9 is a valid CAS Registry Number.

632291-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-5-methylidene-4-(2-phenylethyl)-1,3-dioxolan-2-one

1.2 Other means of identification

Product number -
Other names 4-Methyl-5-methylene-4-(2-phenylethyl)-1,3-dioxolan-2-one

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:632291-67-9 SDS

632291-67-9Relevant academic research and scientific papers

Synthesis of annulated oxazolidinones as potential precursors of cyclic cis-β-amino alcohols

Chudinov,Gashev,Chernysheva,Semenov

, p. 123 - 136 (2007/10/03)

A simple method for the synthesis of annulated 1,3-oxazolidin-2-ones from accessible ketones, acetylene, and carbon dioxide was developed. If their molecules contain arylalkyl substituents, intramolecular cyclization in acidic media gave rise to fused heterocyclic systems in high yields. The effects of the substituents in positions 3 and 5 of the oxazolidine ring on the regioselectivity of this cyclization were studied. The possibilities of converting oxazolidinones into cyclic cis-β-amino alcohols were studied.

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