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3-Phenylpropionic acid, 2-tetrahydrofurylmethyl ester, also known as 2-tetrahydrofuryl methyl 3-phenylpropionate, is a chemical compound with the molecular formula C14H16O3. It is an ester derivative of 3-phenylpropionic acid, where the carboxylic acid group is esterified with 2-tetrahydrofuryl methyl alcohol. 3-Phenylpropionic acid, 2-tetrahydrofurylmethyl ester is characterized by its aromatic phenyl group and a cyclic tetrahydrofuran ring, which contributes to its unique chemical properties. It is often used in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical structure and reactivity. The ester linkage in 3-Phenylpropionic acid, 2-tetrahydrofurylmethyl ester can participate in various chemical reactions, making it a valuable intermediate in organic synthesis.

4647-36-3

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4647-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4647-36-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,4 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4647-36:
(6*4)+(5*6)+(4*4)+(3*7)+(2*3)+(1*6)=103
103 % 10 = 3
So 4647-36-3 is a valid CAS Registry Number.

4647-36-3SDS

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 oxolan-2-ylmethyl 3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names Tetrahydro-2-furanylmethyl 3-phenylpropanoate

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:4647-36-3 SDS

4647-36-3Downstream Products

4647-36-3Relevant academic research and scientific papers

Facile oxidative conversion of alcohols to esters using molecular iodine

Mori, Naoshi,Togo, Hideo

, p. 5915 - 5925 (2007/10/03)

A simple, efficient, and high-yield procedure for the oxidative conversion of alcohols to various types of esters and ketones, with molecular iodine and potassium carbonate was successfully carried out.

A Convenient Protocol for the Esterification of Carboxylic Acids with Alcohols in the Presence of di-t-Butyl Dicarbonate

Goo?en, Lukas J.,D?hring, Arno

, p. 263 - 266 (2007/10/03)

Stoichiometric mixtures of carboxylic acids and primary or secondary alkyl alcohols are cleanly converted into their corresponding esters by treatment with di-t-butyl dicarbonate [(BOC)2O] in the presence of catalytic amounts of N,N′-dimethylaminopyridine (DMAP). This convenient procedure provides a general access to a broad variety of esters including those bearing highly sensitive functional groups such as phenol esters or BOC-groups. Purification of the products is particularly easy since the byproducts t-BuOH and CO2 are volatile - a great advantage over the standard DCC/DMAP method.

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