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5454-11-5

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5454-11-5 Usage

Description

PHENYLETHYL-HEPTANOATE, also known as phenylethyl caproate, is an ester compound characterized by its sweet, fruity, and floral aroma. It is naturally found in various fruits and flowers such as apples, strawberries, and jasmine. This colorless to pale yellow liquid is synthesized through the reaction of phenylethanol and heptanoic acid, and is valued for its long-lasting scent and pleasant fragrance profile.

Uses

Used in Fragrance Industry:
PHENYLETHYL-HEPTANOATE is used as a fragrance ingredient for its sweet, fruity, and floral aroma, enhancing the scent of perfumes, cosmetics, and personal care products.
Used in Food and Beverage Industry:
PHENYLETHYL-HEPTANOATE is used as a flavoring agent to add a pleasant aroma to food products and beverages.

Check Digit Verification of cas no

The CAS Registry Mumber 5454-11-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5454-11:
(6*5)+(5*4)+(4*5)+(3*4)+(2*1)+(1*1)=85
85 % 10 = 5
So 5454-11-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H22O2/c1-2-3-4-8-11-15(16)17-13-12-14-9-6-5-7-10-14/h5-7,9-10H,2-4,8,11-13H2,1H3

5454-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylethyl heptanoate

1.2 Other means of identification

Product number -
Other names phenethyl heptanoate

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:5454-11-5 SDS

5454-11-5Downstream Products

5454-11-5Relevant articles and documents

Staudinger’s phosphazene as an efficient esterifying reagent

Dinesh, Murugan,Ranganathan, Raja,Archana, Sivasubramaniyan,Sathishkumar, Murugan,Roshan Banu, Mohamed Sulthan,Ponnuswamy, Alagusundaram

supporting information, p. 1454 - 1460 (2016/09/14)

A new application of Staudinger’s phosphazene as an efficient esterifying reagent is reported. Staudinger’s phosphazene formed in situ by the reaction of organic mono-azide with triphenylphosphine, which is trapped by carboxylic acid, to afford amide exclusively. In contrast, interestingly the same phosphazene behaves in a different way as an efficient esterifying reagent, affording ester under a solvent-free microwave-assisted protocol wherein alcohol is added as the another component in addition to the other reactants. This discovery adds yet another new application of Staudinger’s phosphazene to synthetic chemistry.

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