131177-53-2

Basic information

• Product Name: (R)-(-)-2-AMINO-6-PHOSPHONOHEXANOIC ACID HYDRATE
• Synonyms: D-AP6;D(-)-2-AMINO-6-PHOSPHONOHEXANOIC ACID;(R)-(-)-2-AMINO-6-PHOSPHONOHEXANOIC ACID HYDRATE;(R)-(-)-2-Amino-6-phosphonohexanoicacidhydrate,e.e.;6-Phosphono-D-norleucine.;(R)-(-)-2-AMINO-6-PHOSPHONOHEXANOIC ACID HYDRATE 95% (97% E.E.);(R)-(-)-2-Amino-6-phosphonohexanoic acid hydrate, 97% ee;BING2
• CAS NO: 131177-53-2
• Molecular Formula: C6H14NO5P
• Molecular Weight: 211.15
• Mol File: 131177-53-2.mol
• Article Data: 6

Chemical Properties

• Melting Point: 215-220 °C
• Boiling Point: 479.3 °C at 760 mmHg
• Flash Point: 243.6 °C
• Appearance: white hygroscopic powder
• Density: 1.452 g/cm³
• Vapor Pressure: 1.67E-10mmHg at 25°C
• Storage Temp.: -20°C
• CAS DataBase Reference: (R)-(-)-2-AMINO-6-PHOSPHONOHEXANOIC ACID HYDRATE(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(-)-2-AMINO-6-PHOSPHONOHEXANOIC ACID HYDRATE(131177-53-2)
• EPA Substance Registry System: (R)-(-)-2-AMINO-6-PHOSPHONOHEXANOIC ACID HYDRATE(131177-53-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 37/39-26-36
• Hazardous Substances Data: 131177-53-2(Hazardous Substances Data)

Usage

Chemical Properties

white fine crystalline powder

InChI:InChI=1/C6H14NO5P/c7-5(6(8)9)3-1-2-4-13(10,11)12/h5H,1-4,7H2,(H,8,9)(H2,10,11,12)/p-2/t5-/m1/s1

Upstream product

• 78944-89-5 6-Phosphono-DL-norleucine 
• 57591-61-4 methyl (R)-2-amino-2-(4-hydroxyphenyl)acetate hydrochloride 
• 5183-27-7 6-bromo-2-acetamido-2-ethoxycarbonyl-hexanoic acid ethyl ester 
• 137622-47-0 2-Acetylamino-2-(4-phosphono-butyl)-malonic acid diethyl ester 
• 114967-67-8 (N-acetylamino-5 bis-ethoxycarbonyl-5,5)-pentylphosphonate de diethyle 

Relevant articles and documents

OPTICALLY-ACTIVE 2-AMINO-PHOSPHONOALKANE ACID, OPTICALLY-ACTIVE 2-AMINOPHOSPHONOALKANE ACID SALT, AND HYDRATES OF THESE

A novel compound has pharmacological activities comparable to those of Nahlsgen and is storable excellently stably. The compound can be produced by a method according to the present invention for producing an optically active 2-amino-phosphonoalkanoic acid salt. In the method, a starting material DL-2-amino-phosphonoalkanoic acid represented by Formula (1) or a hydrate thereof is reacted with an optically active basic compound other than an optically active lysine, to give a diastereomeric salt mixture including a first salt (including a hydrate salt) between a D-2-amino-phosphonoalkanoic acid represented by Formula (1-1) and the optically active basic compound, and a second salt (including a hydrate salt) between an L-2-amino-phosphonoalkanoic acid represented by Formula (1-2) and the optically active basic compound. The diastereomeric salt mixture is fractionally crystallized to isolate one of the first and second diastereomeric salts.

Enantioselective synthesis of both enantiomers of 2-amino-6-phosphonohexanoic acid [(R)- and (S)-AP6], a potent and specific agonist of AMPA receptor subtype

The preparation of both enantiomers of 2-amino-6-phosphonohexanoic acid [(R)- and (S)-AP6] is described. The highly diastereoselective alkylation of imidazolidinones 4 and hydrolysis of the alkylated products [(2R,5R,1'S)-6 and (2S,5S,1'S)-6] proceeds under relatively mild conditions to give the physiologically important, enantiopure aminophosphonic acids (R)-AP6 and (S)-AP6.

PHOSPHORUS-CONTAINING AMINOCARBOXYLIC ACIDS. COMMUNICATION IV. A CONVENIENT METHOD OF PHOSPHONIC ACIDS SYNTHESIS

The communication is concerned with the synthesis of phosphonic aminocarboxylic acids by phosphorylation of diethyl ω-halogen alkyl acetamidomalonates with tris(trimethylsilyl) phosphite, followed by alcoholysis and acid hydrolysis of the resulting intermediate esters.Key words: Phosphonic aminocarboxylic acids; tris(trimethylsilyl) phosphite; ω-halogenalkyl acetamidomalonates; phosphorylation; alcoholysis, hydrolysis