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1-Propen-1-one, 3-phenyl-, also known as 1-phenylprop-1-en-1-one or cinnamaldehyde, is an organic compound with the chemical formula C9H8O. It is a colorless to pale yellow liquid with a strong, pungent odor. Cinnamaldehyde is a key component in the essential oil of cinnamon, contributing to its characteristic aroma and flavor. It is widely used in the food and beverage industry as a flavoring agent, as well as in the perfumery and pharmaceutical industries. The compound is also known for its antimicrobial and anti-inflammatory properties, making it a potential candidate for various therapeutic applications.

87101-44-8

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87101-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87101-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,0 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87101-44:
(7*8)+(6*7)+(5*1)+(4*0)+(3*1)+(2*4)+(1*4)=118
118 % 10 = 8
So 87101-44-8 is a valid CAS Registry Number.

87101-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylprop-1-en-1-one

1.2 Other means of identification

Product number -
Other names 1-Propen-1-one,3-phenyl

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:87101-44-8 SDS

87101-44-8Upstream product

87101-44-8Relevant academic research and scientific papers

Trimethylsilyl Cyanide - A Reagent for Umpolung, VIII. Derivatives of 2-(Trimethylsilyloxy)-2-propenenitrile. Syntheses and General Properties

Hertenstein, Ulrich,Huenig, Siegfried,Reichelt, Helmut,Schaller, Rainer

, p. 261 - 287 (2007/10/02)

Rather different derivatives of the new title compuond 7 were synthesized by routes A - H (Table 2 and 3).The effects of substituents and reaction routes on the E/Z ratios (NMR) is discussed.Replacement of SiMe3 in 7 by RCO- and MeSO2- yields other alkenes with donor (O - X) and acceptor groups (CN) at the same C-atom.Their opposite effects on the β-C-atom is estimated from the corresponding 1H- and 13C-NMR signals.

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