58810-67-6

Basic information

• Product Name: 4(S)-Amino-chroman-3(S)-ol
• Synonyms: 4(S)-Amino-chroman-3(S)-ol;2H-1-Benzopyran-3-ol, 4-aMino-3,4-dihydro-, (3R,4R)-rel-;trans-4-aminochroman-3-ol
• CAS NO: 58810-67-6
• Molecular Formula: C₉H₁₁NO₂
• Molecular Weight: 165.18914
• Mol File: 58810-67-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 112 °C(Solv: ethyl acetate (141-78-6))
• Boiling Point: 300.7±42.0 °C(Predicted)
• Appearance: /
• Density: 1.252±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C(protect from light)
• PKA: 13.99±0.40(Predicted)
• CAS DataBase Reference: 4(S)-Amino-chroman-3(S)-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4(S)-Amino-chroman-3(S)-ol(58810-67-6)
• EPA Substance Registry System: 4(S)-Amino-chroman-3(S)-ol(58810-67-6)

Safety Data

• Hazardous Substances Data: 58810-67-6(Hazardous Substances Data)

Usage

General Description

4(S)-Amino-chroman-3(S)-ol, also known as vitamin E, is a potent antioxidant that is essential for the functioning of the human body. It plays a crucial role in protecting cells from damage caused by free radicals and oxidative stress, thereby reducing the risk of chronic diseases and aging. Vitamin E also supports immune function, skin health, and proper blood clotting. It can be found in various foods such as nuts, seeds, and vegetable oils, and is also available as a dietary supplement. Overall, 4(S)-Amino-chroman-3(S)-ol is an important chemical compound that contributes to overall health and well-being.

Upstream product

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

Downstream Products

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

Relevant articles and documents

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

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.

Synthesis of [1]benzopyrano[3,4 b][1,4]oxazines as potential antidepressants

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