15967-72-3

Basic information

• Product Name: 1,2-Propanediamine, (S)-
• CAS NO: 15967-72-3
• Molecular Formula: C3H10N2
• Molecular Weight: 74.1258
• Mol File: 15967-72-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-Propanediamine, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Propanediamine, (S)-(15967-72-3)
• EPA Substance Registry System: 1,2-Propanediamine, (S)-(15967-72-3)

Safety Data

• Hazardous Substances Data: 15967-72-3(Hazardous Substances Data)

Usage

Chiral compound

Has a non-superimposable mirror image

Applications

Used as a building block in the synthesis of pharmaceuticals, agrochemicals, and polymers

Use as a cross-linking agent

In the production of epoxy resins and polyurethanes

Importance as an intermediate

In the production of chiral materials and pharmaceuticals

Safety precautions

Can cause irritation to the skin, eyes, and respiratory system if proper precautions are not taken.

Upstream product

• 78-90-0 1,2-diaminopropan 
• 19777-66-3 (R)-propane-1,2-diamine dihydrochloride 
• 122833-55-0 (R)-2-Ethoxy-4-methyl-4,5-dihydro-1H-imidazole 

Downstream Products

• 41013-25-6 (2S)-[N,N'-bis(2'-hydroxybenzylidene)]-1,2-diaminopropane 
• 19237-25-3 bis-(salicylidene)-D(-)-propylenediamine 
• 72098-54-5 N¹,N²-dibenzylidene-1,2-propanediamine 
• 75040-70-9 N¹,N²-dibenzyl-1,2-propanediamine 
• 72098-53-4 N¹-benzyl-1,2-propanediamine 
• 122920-65-4 (R)-1.2-bis-benzamino-propane 
• 15250-41-6 (S)-N,N,N',N'-tetrakis[(hydroxycarbonyl)methyl]-1,2-diaminopropane 

Relevant articles and documents

Polymethacrylic zinc porphyrin: A new approach to chiral recognition

A methacrylic homopolymer bearing in the side-chain achiral zinc tetraarylporphyrin moieties, has been studied as macromolecular chromophoric host to determine the absolute configuration of α,ω-diamines. The polymeric material resulted able to bind the ch

SYNTHESIS OF CHIRAL 1,2-DIAMINES

(1'S,5R,S)-(1'-phenyleth-1'-yl)-5-iodomethyl-imidazolines 4a, b have been synthesised and easily resolved by silica gel chromatography.The correlation between the configuration and the 1H-NMR chemical shifts allows to assign the configuration at the C-5 of these intermediates.Each pure diastereomer has been converted to R(-)- and to S(+)-1,2-propyldiamine, respectively.