17966-65-3

Basic information

• Product Name: N-(2-Phenylacetyl)alanine
• Synonyms: N-(2-Phenylacetyl)alanine
• CAS NO: 17966-65-3
• Molecular Formula: C₁₁H₁₃NO₃
• Molecular Weight: 207.22582
• Mol File: 17966-65-3.mol
• Article Data: 8

Chemical Properties

• Melting Point: 150.5-151 °C
• Boiling Point: 467.7±38.0 °C(Predicted)
• Appearance: /
• Density: 1.199±0.06 g/cm3(Predicted)
• PKA: 3.58±0.10(Predicted)
• CAS DataBase Reference: N-(2-Phenylacetyl)alanine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-Phenylacetyl)alanine(17966-65-3)
• EPA Substance Registry System: N-(2-Phenylacetyl)alanine(17966-65-3)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 17966-65-3(Hazardous Substances Data)

Upstream product

• 302-72-7 rac-Ala-OH 
• 103-80-0 phenylacetyl chloride 
• 816-66-0 4-methyl-2-oxopentanoic acid 
• 65415-02-3 Phac-DL-Ala-NH₂ 
• 718-07-0 N-(Phenylacetyl)-L-alanine 

Downstream Products

• 41109-05-1 N-Phenylacetyl alanine methyl ester 
• 58482-85-2 2-benzyl-4-methyl-4H-oxazolin-5-one 
• 859800-39-8 (+/-)-β,β-diethoxy-α-(2-phenyl-acetylamino)-isobutyric acid 
• 108463-01-0 N-(1-Cyclohexyl-3,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-pyridin-3-yl)-2-phenyl-acetamide 
• 143947-57-3 3-(N-Phenylacetylamino)-4-(4-oxobenzopyran-3-yl)-3-methyl-N-p-tolylazetidin-2-one 
• 25637-52-9 2-phenylacetamidoacrylic acid 
• 21149-16-6 N-(Phenylacetyl)dehydroalanine methyl ester 
• 64562-97-6 C₁₂H₁₄ClNO₃ 
• 62191-01-9 3-(2-benzyl-4-methyl-5-oxo-4,5-dihydro-oxazol-4-yl)-2-isothiocyanato-3-methyl-butyric acid ethyl ester 
• 62190-97-0 2,4-dibenzyl-4-methyl-4H-oxazol-5-one 
• 130325-37-0 (S)-1-(N-phenylacetylamino)ethylphosphonic acid 

Relevant articles and documents

Racemization method of chiral N-phenylacetyl amino acid and derivatives thereof

The invention belongs to the field of amino acid racemization, and in particular discloses a racemization method of chiral N-phenylacetyl amino acid and derivatives thereof. The method comprises the following steps: heating phenylacetic acid up to 160-180

Regioselective synthesis of tetrasubstituted pyrroles by 1,3-dipolar cycloaddition and spontaneous decarboxylation

We developed a novel regioselective synthesis of tetrasubstituted pyrroles via the classic 1,3-dipolar cycloaddition of α,β-unsaturated benzofuran-3(2H)-one and azlactones (1) followed by spontaneous decarboxylation. The complete regiochemical control of tetrasubstituted pyrroles was confirmed by the orthogonal synthesis of complementary regioisomers (7a and 7b) simply by using different azlactones (1a and 1b, respectively).

SYNTHESIS OF PEPTIDES WITH α,β-DEHYDROAMINO ACIDS. PART VII. ATTEMPTED SYNTHESIS OF Nα-PHENYLACETYL-α,β-DEHYDRODIPEPTIDES

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