270263-02-0

Basic information

• Product Name: (S)-3-AMINO-5-HEXENOIC ACID HYDROCHLORIDE
• Synonyms: H-BETA-HOGLY(ALLYL)-OH HCL;H-ALGLY-(C*CH2)OH HCL;RARECHEM AK PT 0009;(S)-3-AMINO-5-HEXENOIC ACID HCL;(S)-3-AMINO-5-HEXENOIC ACID HYDROCHLORIDE;H-b-HoGly(allyl)-OH·HCl;(S)-3-Amino-5-hexenoicacidCl;H-β-HoGly(Allyl)-OH.HCl
• CAS NO: 270263-02-0
• Molecular Formula: C6H12ClNO2
• Molecular Weight: 165.62
• Product Categories: 3-Amino-4-phenylbutyric Acid Analogs;3-Amino-4-phenylbutanoic Acid Analogs;B-Amino
• Mol File: 270263-02-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 245℃
• Flash Point: 102℃
• Appearance: /
• Density: 1.064
• Vapor Pressure: 0.00978mmHg at 25°C
• PKA: 3.78±0.10(Predicted)
• CAS DataBase Reference: (S)-3-AMINO-5-HEXENOIC ACID HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-AMINO-5-HEXENOIC ACID HYDROCHLORIDE(270263-02-0)
• EPA Substance Registry System: (S)-3-AMINO-5-HEXENOIC ACID HYDROCHLORIDE(270263-02-0)

Safety Data

• Hazardous Substances Data: 270263-02-0(Hazardous Substances Data)

Usage

Uses

(S)-3-Amino-5-hexenoic acid, HCl

InChI:InChI=1/C6H11NO2.ClH/c1-2-3-5(7)4-6(8)9;/h2,5H,1,3-4,7H2,(H,8,9);1H/t5-;/m0./s1

Upstream product

• 141943-64-8 (±)-2-acetamidohex-5-enoic acid 
• 122471-00-5 acetylamino-3-butenyl-propanedioic acid diethyl ester 
• 276699-69-5 2-allyl-2,3-dihydro-1H-pyridin-4-one 
• 82448-91-7 (R)-3-(2,2,2-Trichloro-ethoxycarbonylamino)-hex-5-enoic acid 
• 82448-88-2 (R)-1-[1,3]Dithian-2-ylmethyl-but-3-enylamine 
• 82448-89-3 ((R)-1-[1,3]Dithian-2-ylmethyl-but-3-enyl)-carbamic acid 2,2,2-trichloro-ethyl ester 
• 82448-90-6 [(R)-1-(2-Oxo-ethyl)-but-3-enyl]-carbamic acid 2,2,2-trichloro-ethyl ester 

Downstream Products

• 1072488-52-8 F-moc-protected 3-amino-2-hexenoic acid 

Relevant articles and documents

Homoallylglycine residues are superior precursors to orthogonally modified thioether containing polypeptides

Homoallylglycine N-carboxyanhydride, Hag NCA, monomers were synthesized and used to prepare polypeptides containing Hag segments with controllable lengths of up to 245 repeats. Poly(l-homoallylglycine), GHA, was found to adopt an α-helical conf

AN ENANTIOSELECTIVE ROUTE TO AN INTERMEDIATE OF THE CARBAPENAM SYSTEM FROM THE CHIRAL γ-BUTYROLACTONE

A new enantioselective synthesis of the keto ester(16) containing β-lactam ring system has been developed using the chiral lactone(1) as a starting material.