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5349-55-3

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5349-55-3 Usage

General Description

Allyl lactate is a chemical compound that belongs to the class of organic compounds known as alpha-hydroxyaldehydes. It is a colorless liquid with a characteristic fruity odor, often used as a food flavoring agent. Allyl lactate is also used in the production of perfumes and as a raw material in the synthesis of other chemicals. It is considered a safe ingredient for use in food and cosmetic products, with low toxicity and minimal adverse health effects. Overall, allyl lactate is a versatile compound with numerous industrial applications and is commonly used in the fragrance and food industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5349-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5349-55:
(6*5)+(5*3)+(4*4)+(3*9)+(2*5)+(1*5)=103
103 % 10 = 3
So 5349-55-3 is a valid CAS Registry Number.

5349-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-enyl 2-hydroxypropanoate

1.2 Other means of identification

Product number -
Other names Propanoic acid, 2-hydroxy-, 2-propenyl ester

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:5349-55-3 SDS

5349-55-3Relevant articles and documents

Ni-Catalyzed C(sp3)–O Arylation of α-Hydroxy Esters

Monteith, John J.,Rousseaux, Sophie A. L.

supporting information, p. 9485 - 9489 (2021/12/09)

A Negishi cross-coupling of α-hydroxy ester derivatives and arylzinc reagents has been developed. This reaction tolerates both primary and secondary C(sp3)–O alcohol precursors and achieves efficient cross-coupling under Ni catalysis without the need for added external metal reductant, photocatalyst, or additives. The arylation of readily accessible C(sp3)–O electrophiles in this operationally simple, rapid, and mild reaction provides a complementary way of accessing desirable α-aryl ester products.

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