5665-74-7

Usage

Uses

Used in Chemical Synthesis:
DL-2-AMINO-1-HEXANOL is used as a building block for the synthesis of various organic compounds and pharmaceuticals. Its versatile structure allows for the creation of a wide range of molecules with different functionalities, making it a valuable component in the development of new drugs and chemicals.
Used in Pharmaceutical Industry:
DL-2-AMINO-1-HEXANOL is used as an intermediate in the production of pharmaceuticals. Its unique structure and reactivity make it a suitable candidate for the development of new drugs with specific therapeutic properties.
Used in Cosmetics Industry:
DL-2-AMINO-1-HEXANOL is used as a component in the formulation of cosmetics, particularly in personal care products. Its properties may contribute to the development of products with improved skin compatibility and enhanced efficacy.
Used in Research and Development:
DL-2-AMINO-1-HEXANOL is used as a research compound for studying its properties and potential applications in various fields. The ion mobility spectrometry (IMS) studies at high temperatures provide valuable insights into its behavior and reactivity, which can be applied to develop new technologies and products.

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 
• 39978-46-6 DL-norleucine ethyl ester 
• 73397-68-9 1-hydroxyhexan-2-one 
• 3844-54-0 norleucine methyl ester hydrochloride 
• 55704-80-8 1-acetoxy-2-chloro-hexane 

Downstream Products

• 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 
• 1609164-47-7 (rac)-8-(cyclohexylmethoxy)-N-(1-hydroxyhexan-2-yl)-2-methylimidazo[1,2-a]pyridine-3-carboxamide 
• 1380510-06-4 C₂₄H₂₄Cl₂F₃N₅O₃ 
• 116905-61-4 2-butyl-N-tosylaziridine 
• 247567-06-2 2-[1-(1-Hydroxymethyl)pentylamino]-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide 
• 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 

Relevant academic research and scientific papers

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.

Amino alcohol derivatives, method of producing said derivatives and medicaments containing them

Compounds of formula I in which R1denotes hydrogen or methyl R2denotes lower straight-chained or branched alkyl with 1 to 10 carbon atoms R3denotes hydrogen or lower alkyl n denotes 0-12 R4denotes alkyl, alkenyl or alkinyl with 6 to 24 carbon atoms, processes for the production thereof as well as pharmaceutical agents containing these compounds for the treatment of osteoporosis.