840507-32-6

Basic information

• Product Name: (2S,3S)-3-DIBENZYLAMINO-5-METHYLHEXANE-1,2-DIOL
• Synonyms: (2S,3S)-3-DIBENZYLAMINO-5-METHYLHEXANE-1,2-DIOL
• CAS NO: 840507-32-6
• Molecular Formula: C21H29NO2
• Molecular Weight: 327.46
• Product Categories: pharmacetical
• Mol File: 840507-32-6.mol

Chemical Properties

• Boiling Point: 487.3°C at 760 mmHg
• Flash Point: 237.4°C
• Appearance: /
• Density: 1.084g/cm³
• Vapor Pressure: 2.6E-10mmHg at 25°C
• Refractive Index: 1.572
• CAS DataBase Reference: (2S,3S)-3-DIBENZYLAMINO-5-METHYLHEXANE-1,2-DIOL(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-3-DIBENZYLAMINO-5-METHYLHEXANE-1,2-DIOL(840507-32-6)
• EPA Substance Registry System: (2S,3S)-3-DIBENZYLAMINO-5-METHYLHEXANE-1,2-DIOL(840507-32-6)

Safety Data

• Hazardous Substances Data: 840507-32-6(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(2S,3S)-3-DIBENZYLAMINO-5-METHYLHEXANE-1,2-DIOL is used as a chiral building block for the synthesis of complex organic molecules, leveraging its unique stereochemistry and functional groups to create a variety of compounds with specific properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2S,3S)-3-DIBENZYLAMINO-5-METHYLHEXANE-1,2-DIOL serves as a key intermediate in the development of pharmaceutical compounds, potentially contributing to the creation of new drugs with improved efficacy and selectivity.
Used in Biochemical Research:
(2S,3S)-3-DIBENZYLAMINO-5-METHYLHEXANE-1,2-DIOL is utilized as a research tool in biochemical studies, where its specific structural features can aid in understanding molecular interactions, enzymatic activities, and biological processes.

InChI:InChI=1/C21H29NO2/c1-17(2)13-20(21(24)16-23)22(14-18-9-5-3-6-10-18)15-19-11-7-4-8-12-19/h3-12,17,20-21,23-24H,13-16H2,1-2H3/t20-,21+/m0/s1

Upstream product

• 871948-88-8 (2R,3S)-O,O-diacetyl-3-dibenzylamino-5-methylhexane-1,2-diol 
• 871948-93-5 (2R,3S)-O¹-acetyl-3-(dibenzylamino)-5-methylhexane-1,2-diol 
• 871949-00-7 (2S,3S)-O¹-acetyl-3-(dibenzylamino)-5-methylhexane-1,2-diol 
• 952526-14-6 (4R)-4-[(S)-1-(dibenzylamino)-3-methylbutyl]-1,3-dioxolan-2-one 
• 171962-77-9 Dibenzyl-((S)-3-methyl-1-(S)-oxiranyl-butyl)-amine 
• 952526-18-0 (4S)-4-[(S)-1-(dibenzylamino)-3-methylbutyl]-1,3-dioxolan-2-one 
• 171815-93-3 (2R,1'S)-2-[1-(dibenzylamino)-3-methylbutyl]oxirane 

Relevant articles and documents

Totally selective reaction of CO2 with enantiopure amino epoxides under mild reaction conditions. Synthesis and synthetic applications of enantiopure (4R, 1′S)- or (4S,1′S)-4-(1-aminoalkyl)-2-oxo-1,3- dioxolanes

(Chemical Equation Presented) The reaction of chiral (2R,1′S)- or (25,1′S)-2-(1-aminoalkyl)epoxides 1 or 2 with CO2, generated from acidic treatment of an aqueous solution of NaHCO3 at room temperature, efficiently afforded enantiopu

Totally selective ring-opening of amino epoxides with ketones: A general entry to enantiopure (2R,3S)- and (2S,3S)-3-aminoalkano-1,2-diols

(Chemical Equation Presented) Transformation of enantiopure diastereoisomers (2R,1′S)- and (2S,1′S)-2-(1-aminoalkyl)epoxides into the corresponding 4-(1-aminoalkyl)-1,3-dioxolanes is achieved by reaction with different ketones in the presence of BF3

Total selective synthesis of enantiopure O1-acyl-3-aminoalkane- 1,2-diols by ring opening of aminoepoxides with carboxylic acids

Synthesis of (2R,3S)- or (2S,3S)-O1-acyl-3-aminoalkane-1,2-diols by ring opening of enantiopure (2R,1′S)- or (2S,1′S)-2-(1- aminoalkyl)epoxides 1 or 2, with carboxylic acids in the presence of BF 3·Et2O and chlorotrimethyl