58810-67-6

Usage

Uses

Used in Healthcare Industry:
4(S)-Amino-chroman-3(S)-ol is used as a dietary supplement for its antioxidant properties, which help in protecting cells from damage caused by free radicals and oxidative stress. This contributes to reducing the risk of chronic diseases and the aging process.
4(S)-Amino-chroman-3(S)-ol is used as a nutrient in the healthcare industry to support immune function, skin health, and proper blood clotting. Its presence in various food sources and dietary supplements ensures that individuals can maintain optimal health and well-being.
Used in Food Industry:
4(S)-Amino-chroman-3(S)-ol is used as a natural antioxidant in the food industry to extend the shelf life of products and maintain their quality. Its presence in nuts, seeds, and vegetable oils contributes to the overall health benefits of these food items.
4(S)-Amino-chroman-3(S)-ol is used as a functional ingredient in the food industry to enhance the nutritional value of products and provide additional health benefits to consumers. Its antioxidant properties and support for immune function, skin health, and blood clotting make it a valuable component in various food products.

Upstream product

• 74736-89-3 (+/-)-3-hydroxy-2,3-dihydro-4H-chromen-4-one 
• 318463-61-5 4-chromanone α-hydroxyoxime 
• 28619-76-3 3-bromo-4-chromanol 
• 491-37-2 2,3-dihydro-4H-1-benzopyran-4-one 
• 98592-23-5 3,3-dibromo chroman-4-one 
• 1776-09-6 3-bromochroman-4-one 

Downstream Products

• 58810-83-6 1-phenethyl-(4ar,10bc)-1,2,3,4a,5,10b-hexahydro-chromeno[3,4-b][1,4]oxazine 
• 58810-83-6 1-phenethyl-(4ar,10bt)-1,2,3,4a,5,10b-hexahydro-chromeno[3,4-b][1,4]oxazine 

Relevant academic research and scientific papers

Chemoenzymatic preparation of enantiopure isomers of 4-aminochroman-3-ol and 1-amino-1,2,3,4-tetrahydronaphthalen-2-ol

Enantiomerically pure N-protected cis-4-aminochroman-3-ol (key precursor in the synthesis of novel HIV second-generation protease inhibitors), its trans isomer and both cis- and trans-1-amino-1,2,3,4-tetrahydronaphthalen-2-ol, useful chiral catalysts in o

Gamma-hydroxy-2-(fluoroalkylaminocarbonyl)-1-piperazinepentanamides and uses thereof

γ-Hydroxy-2-(fluoroalkylaminocarbonyl)-1-piperazinepentanamide compounds are inhibitors of HIV protease and inhibitors of HIV replication. These compounds are useful in the prevention or treatment of infection by HV and the treatment of AIDS, either as compounds, pharmaceutically acceptable salts, pharmaceutical composition ingredients, whether or not in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described. These compounds are effective against HIV viral mutants which are resistant to HIV protease inhibitors currently used for treating AIDS and HIV infection.

Indinavir analogues with blocked metabolism sites as HIV protease inhibitors with improved pharmacological profiles and high potency against PI-resistant viral strains

Indinavir analogues with blocked metabolism sites show highly improved pharmacokinetic profiles in animals. The cis-aminochromanol substituted analogues exhibited excellent potency against both the wild-type (NL4-3) virus and protease inhibitor-resistant HIV strains.

Stereoselective hydrogen bromide-promoted hydrogenation of an α-hydroxyoxime

Hydrogen bromide has been demonstrated to provide optimal cis-selectivity in the reduction of 4-chromanone α-hydroxyoxime (25:1 cis/trans) in 94% yield. This reaction is pivotal in the synthesis of cis-aminochromanol. (C) 2000 Elsevier Science Ltd.