What is the Methyl phenylacetate?

Methyl phenylacetate is colourless liquid, while it's Molecular Formula is C9H10O2. colourless liquid Methyl phenylacetate is utilized for partition coefficient measurement experiments. It is mainly used in the flavor industry and in perfumes to impart honey scents. Further, it acts as a precursor to prepare synthetic perfumes. It acts as an acylating agent and involved in the enantioselective acylation of beta-lactam intermediate using penicillin G amidase.

What is the CAS number for Methyl phenylacetate?

The CAS number of Methyl phenylacetate is 101-41-7.

What is Methyl phenylacetate (101-41-7) used for?

Methyl phenylacetate belongs to an ester compound form between the methanol and phenylacetate. It chemical formula is C6H5CH2COOCH3. It is generally found in brandy, capsicum, honey, pepper, some wine, coca and coca products. It is mainly used as a flavouring agent, and is also supplemented into perfumes to enhance honey scents. It can also be used as the precursor for the manufacture of synthetic perfumes. In addition, as an acylating agent, it can participate in the enantioselective acylation reaction of beta-lactam intermediate catalyzed by the penicillin G amidase.InChI:InChI=1/C9H10O2/c1-11-9(10)7-8-5-3-2-4-6-8/h2-6H,7H2,1H3

What is the Methyl phenylacetate?

Methyl phenylacetate is colourless liquid, while it's Molecular Formula is C9H10O2. colourless liquid Methyl phenylacetate is utilized for partition coefficient measurement experiments. It is mainly used in the flavor industry and in perfumes to impart honey scents. Further, it acts as a precursor to prepare synthetic perfumes. It acts as an acylating agent and involved in the enantioselective acylation of beta-lactam intermediate using penicillin G amidase.

What is the CAS number for Methyl phenylacetate?

The CAS number of Methyl phenylacetate is 101-41-7.

What is Methyl phenylacetate (101-41-7) used for?

Methyl phenylacetate belongs to an ester compound form between the methanol and phenylacetate. It chemical formula is C6H5CH2COOCH3. It is generally found in brandy, capsicum, honey, pepper, some wine, coca and coca products. It is mainly used as a flavouring agent, and is also supplemented into perfumes to enhance honey scents. It can also be used as the precursor for the manufacture of synthetic perfumes. In addition, as an acylating agent, it can participate in the enantioselective acylation reaction of beta-lactam intermediate catalyzed by the penicillin G amidase.InChI:InChI=1/C9H10O2/c1-11-9(10)7-8-5-3-2-4-6-8/h2-6H,7H2,1H3

Methyl 2-phenylacetate

Basic information

Product Name:Methyl 2-phenylacetate
CasNo.:101-41-7
MF:C₉H₁₀O₂

Physical and Chemical Properties

Purity:99%
Melting Point:218 °C(lit.)
Appearance:colourless liquid

Inquiry

Product Details

CasNo： 101-41-7

MF： C₉H₁₀O₂

Appearance： colourless liquid

99% Purity Commercial production Methyl 2-phenylacetate 101-41-7 with Cheapest Price

Molecular Formula:C9H10O2
Molecular Weight:150.177
Appearance/Colour:colourless liquid
Vapor Pressure:0.129mmHg at 25°C
Melting Point:218 °C(lit.)
Refractive Index:1.507
Boiling Point:218 °C at 760 mmHg
Flash Point:93.9 °C
PSA：26.30000
Density:1.055 g/cm³
LogP:1.40210
IDLH:1008
IDLH:2155
IDLH:2733

Methyl phenylacetate(Cas 101-41-7) Usage

Description	Methyl phenylacetate is an organic compound that is a clear, colorless liquid and the methyl ester of phenylacetic acid. It has the structural formula C6H5CH2COOCH3 and is slightly soluble in water but highly soluble in most organic solvents.
Synthesis and Preparation	Methyl phenylacetate, an organic compound with the structural formula C6H5CH2COOCH3, can be synthesized through hydrolysis and esterification from phenylacetonitrile. Methyl phenylacetate can also be produced from benzyl cyanide through acid hydrolysis in the presence of methanol. Benzyl cyanide is derived from benzyl chloride, an industrial chemical.
Biochem/physiol Actions	Methyl phenylacetate is an organic compound with a strong honey-like odor that has many uses. Methyl phenylacetate is the starting material in manufacture of synthetic perfumes.
Safety Profile	Moderately toxic by ingestion and skin contact. A skin irritant. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS.
Definition	ChEBI: Methyl benzeneacetate is a member of benzenes.
Aroma threshold values	Detection: 25 ppb
Production Plant	DEMEI ELECTRONIC COMMERCE FIRM was established in 2024 and is located in Yiwu, Zhejiang Province. Although it was established not long ago, it has more than ten years of industry experience. The affiliated factory covers an area of 7,000 square meters. In addition, it also has its own excellent reserve of talents. Our high-tech R&D team, workshop production and sales R&D personnel have exceeded 200 people. In recent years, our products have also been exported to the UK, Germany, Australia, the Netherlands, Poland, Russia, Kazakhstan, the Philippines, Malaysia, Singapore and many other regions.
Who Evaluation	Evaluation year: 2002

InChI:InChI=1/C9H10O2/c1-11-9(10)7-8-5-3-2-4-6-8/h2-6H,7H2,1H3

101-41-7 Relevant articles

Enantiocomplementary preparation of (S)- and (R)-mandelic acid derivatives via α-hydroxylation of 2-arylacetic acid derivatives and reduction of α-ketoester using microbial whole cells

Yongzheng Chen a b , Jinggang Xu a , Xiaoying Xu a , Yu Xia a , Hui Lin a , Shiwen Xia a , Lixin Wang a

, Tetrahedron: Asymmetry Volume 18, Issue 21 , 22 October 2007, Pages 2537-2540

Forty one microorganisms belonging to different taxonomical groups were used to carry out the enantioselective reduction of methyl benzoylformate to afford the corresponding (R)-methyl mandelate, with moderate to high ee. In contrast, the monooxygenase enzyme in Helminthosporium sp. CIOC3.3316 catalyzed the hydroxylation of methyl 2-phenylacetate to (S)-methyl mandelate. This combination of oxidation and reduction biotransformations thus provides a method for preparing the enantiomers of chiral α-hydroxy acid derivatives.

Three-component coupling reaction of benzylic halides, carbon dioxide, and N,N-dimethylformamide by using paired electrolysis: Sacrificial anode-free efficient electrochemical carboxylation of benzylic halides

Senboku, Hisanori,Nagakura, Kotaro,Fukuhara, Tsuyoshi,Hara, Shoji

, p. 3850 - 3856 (2015)

Sacrificial anode-free efficient electro...

Chemistry of palladium phosphinite (PPh2(OR)) and phosphonite (P(OPh)2(OH)) complexes: Catalytic activity in methoxycarbonylation and Heck coupling reactions

Pryjomska, Iweta,Bartosz-Bechowski, Hubert,Ciunik, Zbigniew,Trzeciak, Anna M.,Ziolkowski, Jozef J.

, p. 213 - 220 (2006)

The new phosphinite and phosphonite comp...

MICROBIAL HYDROLYSIS AS A POTENT METHOD FOR THE PREPARATION OF OPTICALLY ACTIVE NITRILES, AMIDES AND CARBOXYLIC ACIDS

Kakeya, Hideaki,Sakai, Naoko,Sugai, Takeshi,Ohta, Hiromichi

, p. 1343 - 1346 (1991)

Many kinds of aromatic nitriles have bee...

101-41-7 Upstream products

186581-53-3
diazomethane
103-82-2
phenylacetic acid
67-56-1
methanol
3282-32-4
2-diazo-acetophenone

101-41-7 Downstream products

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68872-03-7
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5460-60-6
N-phenethyl-2-phenylacetamide