5665-74-7

Basic information

• Product Name: DL-2-AMINO-1-HEXANOL
• Synonyms: DL-2-AMINO-1-HEXANOL;DL-NORLEUCINOL;(±)-Norleucinol;2-aminohexan-1-ol;2-azanylhexan-1-ol;DL-2-Amino-1-hexanol 90%, technical grade
• CAS NO: 5665-74-7
• Molecular Formula: C₆H₁₅NO
• Molecular Weight: 117.19
• Product Categories: Amino Alcohols;Building Blocks;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
• Mol File: 5665-74-7.mol
• Article Data: 2

Chemical Properties

• Melting Point: 28.94°C (estimate)
• Boiling Point: 190-192 °C740 mm Hg(lit.)
• Flash Point: 212 °F
• Appearance: /
• Density: 0.912 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.135mmHg at 25°C
• Refractive Index: n20/D 1.4522(lit.)
• CAS DataBase Reference: DL-2-AMINO-1-HEXANOL(CAS DataBase Reference)
• NIST Chemistry Reference: DL-2-AMINO-1-HEXANOL(5665-74-7)
• EPA Substance Registry System: DL-2-AMINO-1-HEXANOL(5665-74-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39
• WGK Germany: 3
• Hazardous Substances Data: 5665-74-7(Hazardous Substances Data)

Usage

General Description

Reduced mobility of protonated DL-2-amino-1-hexanol in air, at 200°C, has been evaluated by ion mobility spectrometry (IMS).

InChI:InChI=1/C6H15NO/c1-2-3-4-6(7)5-8/h6,8H,2-5,7H2,1H3

Upstream product

• 616-06-8 2-amino-hexanoic acid 
• 592-41-6 1-hexene 
• 73397-68-9 1-hydroxyhexan-2-one 
• 3844-54-0 norleucine methyl ester hydrochloride 
• 55704-80-8 1-acetoxy-2-chloro-hexane 
• 39978-46-6 DL-norleucine ethyl ester 

Downstream Products

• 247567-06-2 2-[1-(1-Hydroxymethyl)pentylamino]-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide 
• 137258-12-9 C₁₁H₂₃NO₃ 
• 80696-28-2 (2R)-2-amino-2-butyl-1-ethanol 
• 80696-29-3 (S)-(+)-2-Amino-1-hexanol 
• 145842-49-5 (+/-)-2-benzyloxycarbonylaminohexan-1-ol 
• 1380510-06-4 C₂₄H₂₄Cl₂F₃N₅O₃ 
• 292835-42-8 5-((2S)-2-({(2S)-2-[(tert-Butoxycarbonyl)amino]-3-phenylpropanoyl}amino)-3-{[1-(hydroxymethyl)pentyl]amino}-3-oxopropyl)-2-(carboxymethoxy)benzoic Acid 
• 1025807-23-1 C₁₄H₂₁N₃O₃ 
• 1027283-94-8 [1-(N-Phenyl-hydrazinomethyl)-pentyl]-carbamic acid methyl ester 
• 1026065-02-0 (1-Phenylaminomethyl-pentyl)-carbamic acid methyl ester 
• 750592-66-6 (+/-)-N,N-dibenzyl-2-aminohexan-1-ol 
• 116905-61-4 2-butyl-N-tosylaziridine 
• 1609164-47-7 (rac)-8-(cyclohexylmethoxy)-N-(1-hydroxyhexan-2-yl)-2-methylimidazo[1,2-a]pyridine-3-carboxamide 

Relevant articles and documents

A catalyst-free, convenient construction of eight-membered [1,4]oxazocane-5,8-dione heterocycles from aminoethanols with divinyl succinate

A convenient protocol for the synthesis of [1,4]oxazocane-5,8-dione heterocycles by direct cyclization using 2-substituted aminoethanols and divinyl succinate without any catalysts and additives was established. This strategy is quite simple and effective to obtain eight-membered rings incorporating lactone and lactam functional groups. Georg Thieme Verlag Stuttgart.