37534-65-9

Basic information

• Product Name: N-CARBAMYL-DL-PHENYLALANINE CRYSTALLINE
• Synonyms: N-CARBAMYL-DL-PHENYLALANINE CRYSTALLINE;3-phenyl-2-ureidopropanoic acid
• CAS NO: 37534-65-9
• Molecular Formula: C₁₀H₁₂N₂O₃
• Molecular Weight: 208.21388
• Mol File: 37534-65-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 406.6°Cat760mmHg
• Flash Point: 199.7°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 2.44E-07mmHg at 25°C
• Refractive Index: 1.587
• CAS DataBase Reference: N-CARBAMYL-DL-PHENYLALANINE CRYSTALLINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-CARBAMYL-DL-PHENYLALANINE CRYSTALLINE(37534-65-9)
• EPA Substance Registry System: N-CARBAMYL-DL-PHENYLALANINE CRYSTALLINE(37534-65-9)

Safety Data

• Hazardous Substances Data: 37534-65-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H12N2O3/c11-10(15)12-8(9(13)14)6-7-4-2-1-3-5-7/h1-5,8H,6H2,(H,13,14)(H3,11,12,15)

Upstream product

• 89-24-7 5-phenylimidazolidine-2,4-dione 
• 372-75-8 Citrulline 
• 150-30-1 Phenylalanine 
• 462-60-2 N-carbamoylglycine 
• 590-28-3 potassium cyanate 
• 57-13-6 urea 
• 7732-18-5 water 
• 119290-61-8 (±)‐phenylalanine benzyl ester p-toluenesulfonic acid 
• 63-91-2 L-phenylalanine 

Downstream Products

• 89-24-7 5-phenylimidazolidine-2,4-dione 
• 583-47-1 4-benzyl-oxazolidine-2,5-dione 
• 3530-82-3 5-benzyl-hydantoin 
• 949-45-1 (S)-3-phenyl-2-ureido-propionic acid 
• 54896-72-9 (R)-3-phenyl-2-ureido-propionic acid 
• 63-91-2 L-phenylalanine 

Relevant articles and documents

A practically simple, catalyst free and scalable synthesis of: N -substituted ureas in water

A practically simple, mild and efficient method is developed for the synthesis of N-substituted ureas by nucleophilic addition of amines to potassium isocyanate in water without organic co-solvent. Using this methodology, a variety of N-substituted ureas (mono-, di- and cyclic-) were synthesized in good to excellent yields with high chemical purity by applying simple filtration or routine extraction procedures avoiding silica gel purification. The developed methodology was also found to be suitable for gram scale synthesis of molecules having commercial application in large volumes. The identified reaction conditions were found to promote a unique substrate selectivity from a mixture of two amines.

2-SUBSTITUTED-TRANS-5-ARYL-2,3,4,4a,5,9B-HEXAHYDRO-1H-PYRIDO[4,3-b]INDOLES

2-Substituted-5-aryl-2,3,4,4a,5,9b-hexahydro-1H-pyrido 4,3-b!indoles of the formula (I): STR1 and the pharmaceutically-acceptable salts thereof, wherein the hydrogen atoms in the 4a position and 9b positions are in a trans relationship to each other and t