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Pentan-3-yl benzoate, also known as 3-pentyl benzoate, is an organic compound with the chemical formula C12H16O2. It is a colorless liquid that is soluble in organic solvents and has a fruity, floral odor. This ester is formed by the reaction of pentan-3-ol and benzoic acid, and it is commonly used as a fragrance ingredient in various personal care products, such as perfumes and cosmetics, due to its pleasant scent. Additionally, it may have potential applications in the pharmaceutical and chemical industries.

5436-54-4

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5436-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5436-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5436-54:
(6*5)+(5*4)+(4*3)+(3*6)+(2*5)+(1*4)=94
94 % 10 = 4
So 5436-54-4 is a valid CAS Registry Number.

5436-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name pentan-3-yl benzoate

1.2 Other means of identification

Product number -
Other names Pentyl-(3)-benzoat

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:5436-54-4 SDS

5436-54-4Relevant academic research and scientific papers

Base-catalyzed selective esterification of alcohols with unactivated esters

Zhang, Chunyan,Zhang, Guoying,Luo, Shizhong,Wang, Chunfu,Li, Huiping

supporting information, p. 8467 - 8471 (2018/12/01)

A practical and efficient base-catalyzed esterification has been developed for the facile synthesis of a broad range of esters from simple alcohols with unactivated tert-butyl esters. This protocol could be conducted at mild conditions, providing esters in high to excellent yields with good functional tolerance. Mechanistic studies provided evidence of an exchange of the tert-butyl alkoxide metal with the alcohol, producing a new alkoxide to participate in the transesterification reaction.

Simple method for the preparation of esters from Grignard reagents and alkyl 1-imidazolecarboxylates

Werner, Thomas,Barrett, Anthony G. M.

, p. 4302 - 4304 (2007/10/03)

The reaction of Grignard reagents with alkyl imidazolecarboxylates, which were prepared from alcohols with carbonyl diimidazole, gave the corresponding esters in good to excellent yields. This method conveniently provides esters from alkyl halides and alcohols by C1-carbon chain extension.

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