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5468-06-4

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5468-06-4 Usage

Description

1,3-Dioxolane, 4,5-dimethyl-2-(phenylmethyl)-, also known as Phenylacetaldehyde-2,3-butylene glycol acetal, is an organic compound with a sweet, floral, somewhat earthy fragrance and a fruity flavor. It is commonly used as a flavoring agent and fragrance ingredient in various industries.

Uses

Used in Flavor and Fragrance Industry:
1,3-Dioxolane, 4,5-dimethyl-2-(phenylmethyl)is used as a flavoring agent for its sweet, fruity taste and as a fragrance ingredient for its floral, earthy scent. It is commonly used in the production of food, beverages, cosmetics, and perfumes to enhance their sensory properties and consumer appeal.

Preparation

By condensation of phenylacetaldehyde with 2,3-butylene glycol.

Check Digit Verification of cas no

The CAS Registry Mumber 5468-06-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5468-06:
(6*5)+(5*4)+(4*6)+(3*8)+(2*0)+(1*6)=104
104 % 10 = 4
So 5468-06-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H16ClN3O3/c1-22-14-8-11(9-15(23-2)16(14)24-3)17-19-10-20-21(17)13-6-4-12(18)5-7-13/h4-10H,1-3H3

5468-06-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-4,5-dimethyl-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names FEMA No. 2875

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:5468-06-4 SDS

5468-06-4Relevant articles and documents

Palladium-catalyzed synthesis of terminal acetals via highly selective anti-Markovnikov nucleophilic attack of pinacol on vinylarenes, allyl ethers, and 1,5-dienes

Yamamoto, Mayumi,Nakaoka, Sonoe,Ura, Yasuyuki,Kataoka, Yasutaka

supporting information; experimental part, p. 1165 - 1167 (2012/02/04)

A palladium-catalyzed reaction of vinylarenes, allyl ethers, and 1,5-dienes with pinacol proceeded via a selective anti-Markovnikov nucleophilic attack to afford corresponding terminal acetals as major products. The bulkiness of pinacol was found to be critical in controlling the regioselectivity. The Royal Society of Chemistry 2012.

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