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Cinnamate, also known as cinnamic acid ester, is a class of organic compounds derived from the esterification of cinnamic acid with various alcohols. These compounds are characterized by a phenylpropenoic acid structure, featuring a phenyl ring and a vinyl group attached to a carboxylic acid moiety. Cinnamate is widely found in nature, particularly in plants, and is known for its aromatic properties. It is used in the food and flavoring industry for its distinct sweet, floral, and balsamic scent, and is also employed in the synthesis of various pharmaceuticals and agrochemicals. The versatility of cinnamate compounds makes them valuable in a range of applications, from enhancing food flavors to serving as intermediates in chemical reactions.

4151-45-5

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4151-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4151-45-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,5 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4151-45:
(6*4)+(5*1)+(4*5)+(3*1)+(2*4)+(1*5)=65
65 % 10 = 5
So 4151-45-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/p-1

4151-45-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name cinnamate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid, 3-phenyl-, ion(1-)

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:4151-45-5 SDS

4151-45-5Upstream product

4151-45-5Downstream Products

4151-45-5Relevant academic research and scientific papers

Kinetics and mechanism of the basic hydrolysis of indomethacin and related compounds: A reevaluation

Cipiciani,Ebert,Linda,Rubessa,Savelli

, p. 1075 - 1076 (2007/10/02)

The kinetics of the hydrolysis of indomethacin and related compounds were studied in an alkaline medium at 25°. The pseudo-first-order rate constants were evaluated from log absorbance versus time plots in the ultraviolet. These compounds showed a second-order rate constant at low concentrations of hydroxide ion and a first-order rate constant at higher concentrations of hydroxide ion.

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