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104-65-4

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104-65-4 Usage

Chemical Properties

Cinnamyl formate has a balsamic, fruital-floral odor and bittersweet taste reminiscent of apple.

Occurrence

Reported found in narcissus.

Preparation

By esterification of cinnamyl alcohol with formic acid.

Aroma threshold values

Detection at 1.0%: cinnamon spicy, slightly balsamic, cherry fruity with berry and tropical nuances.

Taste threshold values

Taste characteristics at 5 ppm: sweet, cinnamon-like, astringent, with woody resinous and balsamic nuances.

General Description

Cinnamyl formate is an α,β-unsaturated?ester that can be used as a flavoring agent and a fragrance ingredient.

Flammability and Explosibility

Notclassified

Safety Profile

Moderately toxic by ingestion. See also ESTERS. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes.

Metabolism

Cinnamyl formate is hydrolysed by porcine pancreatic lipase 2.6 times more rapidly than is cinnamyl oleate under identical conditions (Brockerhoff, 1970).

Check Digit Verification of cas no

The CAS Registry Mumber 104-65-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104-65:
(5*1)+(4*0)+(3*4)+(2*6)+(1*5)=34
34 % 10 = 4
So 104-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O2/c11-9-12-8-4-7-10-5-2-1-3-6-10/h1-7,9H,8H2/b7-4+

104-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Cinnamyl Formate

1.2 Other means of identification

Product number -
Other names 2-Propen-1-ol, 3-phenyl-, formate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:104-65-4 SDS

104-65-4Relevant articles and documents

"Counter" Phase Transfer Catalysis by Water-soluble Phosphine Complexes. Catalytic Reduction of Allyl Chlorides and Acetates with Sodium Formate in Two-phase Systems

Okano, Tamon,Moriyama, Yoshiyuki,Konishi, Hisatoshi,Kiji, Jitsuo

, p. 1463 - 1466 (1986)

In the reduction of allyl chlorides and acetates with sodium formate in a heptane-water two-phase system, water-soluble palladium complexes function as a novel type of catalyst which transports the substrate into the aqueous phase and causes it to react with sodium formate.

Efficient Enzymatic Preparation of Flavor Esters in Water

Perdomo, Igor Chiarelli,Gianolio, Stefania,Pinto, Andrea,Romano, Diego,Contente, Martina Letizia,Paradisi, Francesca,Molinari, Francesco

, p. 6517 - 6522 (2019/06/20)

A straightforward biocatalytic method for the enzymatic preparation of different flavor esters starting from primary alcohols (e.g., isoamyl, n-hexyl, geranyl, cinnamyl, 2-phenethyl, and benzyl alcohols) and naturally available ethyl esters (e.g., formate, acetate, propionate, and butyrate) was developed. The biotransformations are catalyzed by an acyltransferase from Mycobacterium smegmatis (MsAcT) and proceeded with excellent yields (80-97%) and short reaction times (30-120 min), even when high substrate concentrations (up to 0.5 M) were used. This enzymatic strategy represents an efficient alternative to the application of lipases in organic solvents and a significant improvement compared with already known methods in terms of reduced use of organic solvents, paving the way to sustainable and efficient preparation of natural flavoring agents.

An Effective Pt-Cu/SiO2 Catalyst for the Selective Hydrogenation of Cinnamaldehyde

Wang, Dong,Zhu, Yujun

, (2018/05/23)

The bimetal catalyst Pt-Cu/SiO2 was prepared by the impregnation method. Its catalytic performance was investigated by the selective hydrogenation of cinnamaldehyde. Pt-Cu/SiO2 exhibited much higher selectivity (64.1%) to cinnamyl al

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