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2-amino-2-oxo-1-phenylethyl acetate, also known as phenylalanine ethyl ester, is an organic compound with the chemical formula C10H13NO3. It is a derivative of phenylalanine, an essential amino acid, and is characterized by the presence of an ester group (-COOCH2CH3) attached to the phenylalanine molecule. 2-amino-2-oxo-1-phenylethyl acetate is a white crystalline solid that is soluble in water and various organic solvents. It is used in the synthesis of pharmaceuticals, as a flavoring agent in the food industry, and as a building block in the production of other chemicals. Phenylalanine ethyl ester is also of interest in research due to its potential applications in the development of new drugs and its role in understanding the biochemistry of amino acids.

6635-16-1

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6635-16-1 Usage

Explanation

Represents the chemical composition of the compound.

Explanation

Another name for 2-amino-2-oxo-1-phenylethyl acetate, which is easier to pronounce and remember.

Explanation

Imparts a pleasant smell, making it valuable in perfumes and food flavorings.

Explanation

Originates from the reaction between two precursor molecules, phenylethylamine and acetic acid.

Explanation

Employed in various industries due to its pleasant aroma and antimicrobial properties.

Explanation

Effective in preventing the growth of certain bacteria and fungi, making it suitable for preservation in personal care products.

Explanation

Serves as a versatile compound with applications in fragrance, flavor, and personal care industries.

Odor

Fruity and Floral

Formation

Combination of Phenylethylamine and Acetic Acid

Perfumes

Provides fragrance notes.

Food Flavorings

Enhances flavor profiles.

Personal Care Products

Acts as an antimicrobial agent.

Antimicrobial Properties

Inhibition of Bacteria and Fungi Growth

Fragrance and Flavor Industries

Valuable for its aromatic properties.

Preservation in Personal Care Products

Used for inhibiting microbial growth.

Check Digit Verification of cas no

The CAS Registry Mumber 6635-16-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6635-16:
(6*6)+(5*6)+(4*3)+(3*5)+(2*1)+(1*6)=101
101 % 10 = 1
So 6635-16-1 is a valid CAS Registry Number.

6635-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-amino-2-oxo-1-phenylethyl) acetate

1.2 Other means of identification

Product number -
Other names 2-amino-2-oxo-1-phenylethyl acetate

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:6635-16-1 SDS

6635-16-1Downstream Products

6635-16-1Relevant academic research and scientific papers

Catalytic Transfer Hydration of Cyanohydrins to α-Hydroxyamides

Kanda, Tomoya,Naraoka, Asuka,Naka, Hiroshi

, p. 825 - 830 (2019/01/14)

We report the palladium(II)-catalyzed transfer hydration of cyanohydrins to α-hydroxyamides by using carboxamides as water donors. This method enables selective hydration of various aldehyde- and ketone-derived cyanohydrins to afford α-mono- and α,α-disubstituted-α-hydroxyamides, respectively, under mild conditions (50 °C, 10 min). The direct conversion of fenofibrate, a drug bearing a benzophenone moiety, into a functionalized α,α-diaryl-α-hydroxyamide was achieved by means of a hydrocyanation-transfer hydration sequence. Preliminary kinetic studies and the synthesis of a site-specifically 18O-labeled α-hydroxyamide demonstrated the carbonyl oxygen transfer from the carboxamide reagent into the α-hydroxyamide product.

Probing the enantioselectivity of a diverse group of purified cobalt-centred nitrile hydratases

Van Pelt,Zhang,Otten,Holt,Sorokin,Van Rantwijk,Black,Perry,Sheldon

experimental part, p. 3011 - 3019 (2011/06/17)

In this study a diverse range of purified cobalt containing nitrile hydratases (NHases, EC 4.2.1.84) from Rhodopseudomonas palustris HaA2 (HaA2), Rhodopseudomonas palustris CGA009 (009), Sinorhizobium meliloti 1021 (1021), and Nitriliruptor alkaliphilus (iso2), were screened for the first time for their enantioselectivity towards a broad range of chiral nitriles. Enantiomeric ratios of >100 were found for the NHases from HaA2 and CGA009 on 2-phenylpropionitrile. In contrast, the Fe-containing NHase from the well-characterized Rhodococcus erythropolis AJ270 (AJ270) was practically aselective with a range of different α-phenylacetonitriles. In general, at least one bulky group in close proximity to the α-position of the chiral nitriles seemed to be necessary for enantioselectivity with all NHases tested. Nitrile groups attached to a quaternary carbon atom were only reluctantly accepted and showed no selectivity. Enantiomeric ratios of 80 and >100 for AJ270 and iso2, respectively, were found for the pharmaceutical intermediate naproxennitrile, and 3-(1-cyanoethyl)benzoic acid was hydrated to the corresponding amide by iso2 with an enantiomeric ratio of >100.

Enantioselective homoallyl-cyclopropanation of dibenzylideneacetone by modified allylindium halide reagents-rapid access to enantioenriched 1-styryl-norcarene

Lloyd-Jones, Guy C.,Wall, Philip D.,Slaughter, Jennifer L.,Parker, Alexandra J.,Laffan, David P.

, p. 11402 - 11412 (2007/10/03)

Dibenzylideneacetone (8) reacts with in situ-generated allylindium halide reagents to yield the product of a homoallyl-cyclopropanation reaction: 2-(3″-butenyl)-1,1-bis[(E)-2′-phenylethenyl]cyclopropane (9), which proceeds via step-wise cleavage of the C{double bond, long}O bond and delivery of two allyl fragments from the reagent. A range of enantiomerically enriched ligands have been tested as stoichiometric asymmetric modifiers for this process. Enantiopure compounds such as cinchona alkaloids, ephedra, aminoalcohols and tartaric acid derivatives, which have proven of utility as asymmetric modifiers for the indium-mediated allylation of aldehydes and ketones, were very inefficient in the process 8→9. However, mandelic acid derivatives, in particular mandelates, were found to be of significant potential. The absolute stereochemistry of the cyclopropane 9 has been determined by degradation to 1,1-dicarboxymethyl-2-butylcyclopropane, converging with an independent enantioselective synthesis starting from hexene. Under optimised conditions, viz. using allylindium iodide reagents and working-up with aqueous Na2SO3 to avoid iodine-mediated polymerisation, (S)-9 can be generated in 86% yield and with (S)-methyl mandelate as modifier useful enantiopurity (94/6 er) was observed. The cyclopropane product ((S)-9) undergoes RCM using standard conditions to afford a norcarene unit ((1S,6S)-1-(E)-2′-(phenylethenyl)-bicyclo[4.1.0]hept-2-ene) without loss of enantiopurity.

Nitrile hydratase activity of a recombinant nitrilase

Fernandes, Bruno C. M.,Mateo, Cesar,Kiziak, Christoph,Chmura, Andrzej,Wacker, Jan,Van Rantwijk, Fred,Stolz, Andreas,Sheldon, Roger A.

, p. 2597 - 2603 (2007/10/03)

Appreciable amounts of amide are formed in the course of nitrile hydrolysis in the presence of recombinant nitrilase from Pseudomonas fluorescens EBC 191, depending on the α-substituent and the reaction conditions. The ratio of the nitrilase and nitrile hydratase activities of the enzyme is profoundly influenced by the electronic and steric properties of the reactant. In general, amide formation increased when the α-substituent was electron-deficient; 2-chloro-2-phenylacetonitrile, for example, afforded 89% amide. We found, moreover, that (R)-mandelo-nitrile was hydrolysed with 11% of amide formation whereas 55% amide was formed from the (S)-enantiomer; a similar effect was found for the O-acetyl derivatives. A mechanism that accomodates our results is proposed.

Catalytic, asymmetric synthesis of α-acetoxy amides

North, Michael,Parkins, Adrian W.,Shariff, Atiya N.

, p. 7625 - 7627 (2007/10/03)

Treatment of aldehydes with a titanium (salen) based catalyst, potassium cyanide and acetic anhydride gives non-racemic cyanohydrin acetates, which undergo chemoselective hydrolysis to α-acetoxy amides when treated with a platinum phosphinito catalyst.

Chemo-enzymatic synthesis of enantiomerically pure (R)-2-naphthylmethoxyacetic acid

Kimura, Mayumi,Kuboki, Atsuhito,Sugai, Takeshi

, p. 1059 - 1068 (2007/10/03)

Enantiomerically pure (R)-2-naphthylmethoxyacetic acid (2-NMA) was synthesized from 2-naphthaldehyde via an integrated chemo-enzymatic procedure. The one-pot, successive use of SnBr2-TMSCN and AcBr worked effectively to give a racemic cyanohydrin acetate. Lipase from Burkholderia cepacia then mediated the highly enantioselective hydrolysis of the (S)-enantiomer of the racemate, leaving the (R)-acetate with an e.e. of >99.9%. The resulting product of this enzyme-catalyzed hydrolysis, an (S)-cyanohydrin, spontaneously decomposed into naphthaldehyde, the starting material of this synthetic route, which could be recycled. The hydration of nitrile to amide as well as the hydrolysis of the acetate was performed with a microorganism, Rhodococcus rhodochrous, under very mild conditions without any loss of the enantiomeric purity. The amide group was hydrolyzed with nitrosylsulfuric acid, and the product was isolated as an α-hydroxy ester. The α-hydroxyl group was methylated with diazomethane-silica gel and the final task, hydrolysis of the ester, was accomplished under conditions as mild as neutral pH with an esterase from Krebsiella oxytoca to give enantiomerically pure 2-NMA.

The Chemistry of 5-Oxodihydroisoxales. XI; The Photolysis of 3-Hydroxy-4-phenylisoxazol-5(2H)-ones (Phenyldisic Acids)

Prager, Rolf H.,Smith, Jason A.

, p. 217 - 226 (2007/10/02)

3-Hydroxy-2-methyl-4-phenylisoxazol-5(2H)-one, 3-hydroxy-2,4-diphenylisoxazol-5(2H)-one and phenyldisic acid have been photolysed at 254 nm in hydroxylic solvents.By comparision of the respective products with those obtained from 3-methoxy-4-phenylisoxazo

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