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Ethyl 3-methyl-3-phenylbutanoate is an organic compound with the chemical formula C13H18O2. It is a colorless liquid with a fruity, apple-like odor and is commonly used as a flavoring agent in the food and beverage industry. This ester is formed by the reaction of ethyl alcohol and 3-methyl-3-phenylbutanoic acid, and it is characterized by its molecular structure, which includes a phenyl group, a methyl group, and a butanoate chain. Ethyl 3-methyl-3-phenylbutanoate is also known as ethyl 3-methylphenylbutyrate and can be found in trace amounts in various fruits, such as apples and pears, contributing to their characteristic aroma. Its use in the flavor industry is due to its ability to mimic natural fruit flavors, enhancing the taste and aroma of products without the need for actual fruit components.

4111-61-9

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4111-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4111-61-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4111-61:
(6*4)+(5*1)+(4*1)+(3*1)+(2*6)+(1*1)=49
49 % 10 = 9
So 4111-61-9 is a valid CAS Registry Number.

4111-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-methyl-3-phenylbutanoate

1.2 Other means of identification

Product number -
Other names 3-Methyl-3-phenyl-buttersaeure-aethylester

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:4111-61-9 SDS

4111-61-9Relevant academic research and scientific papers

Enantioselective halogenative semi-pinacol rearrangement: A stereodivergent reaction on a racemic mixture

Romanov-Michailidis, Fedor,Pupier, Marion,Gune, Laure,Alexakis, Alexandre

supporting information, p. 13461 - 13464 (2015/02/19)

An efficient, quantitative deracemization strategy for optically inactive allylic cycloalkanols has been achieved using the biphasic halogenative semi-pinacol reaction protocol. The resultant β-halo spiroketones, containing three contiguous stereogenic ce

'Me2CuLi·TMSCl in CH2Cl2'. The most powerful methylating agent for sterically congested α,β-enoates

Asao, Naoki,Lee, Sunyoung,Yamamoto, Yoshinori

, p. 4265 - 4266 (2007/10/03)

The reaction of Me2CuLi with sterically congested α,β-unsaturated esters in the presence of TMSCl in CH2Cl2 proceeded very smoothly to produce the conjugate addition products in high yields.

Enantioselective Protonation of Samarium Enolates by a C2-Symmetric Chiral Diol

Takeuchi, Seiji,Ohira, Akiko,Miyoshi, Norikazu,Mashio, Hajime,Ohgo, Yoshiaki

, p. 1763 - 1780 (2007/10/02)

High enantioselectivity (up to 97percentee) have been achieved in the protonation of samarium enolates which were generated by SmI2-mediated cross-coupling reaction between unsymmetrical dialkylketene and allyl iodide, using, using a C2-symmetr

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