2811-20-3

Basic information

• Product Name: 1-Propanol, 2,3-diamino-
• CAS NO: 2811-20-3
• Molecular Formula: C3H10N2O
• Molecular Weight: 90.1252
• Mol File: 2811-20-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-Propanol, 2,3-diamino-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanol, 2,3-diamino-(2811-20-3)
• EPA Substance Registry System: 1-Propanol, 2,3-diamino-(2811-20-3)

Safety Data

• Hazardous Substances Data: 2811-20-3(Hazardous Substances Data)

Usage

General Description

1-Propanol, 2,3-diamino- is a chemical compound with the molecular formula C3H10N2O, also known as 2,3-diaminopropanol. It is a colorless, viscous liquid with a faint amine odor. 1-Propanol, 2,3-diamino- is primarily used as a chemical intermediate in the production of pharmaceuticals, dyes, and other organic compounds. It can also be used as a corrosion inhibitor, an emulsifier, and a stabilizer in various industrial processes. 1-Propanol, 2,3-diamino- is considered to be a hazardous chemical and should be handled with caution due to its potential health hazards and flammability.

Upstream product

• 67880-10-8 2,3-diazido-1-propanol 
• 56-81-5 glycerol 
• 591-87-7 Allyl acetate 
• 638-38-0 manganese triacetate 
• 54798-69-5 3-acetoxy-1,2-bis-acetylamino-propane 
• 101857-37-8 3-methoxy-1,3-propanediamine 

Downstream Products

• 1616860-66-2 2,3-bis((E)-(3,5-di-tert-butyl-2-hydroxybenzylidene)amino)propan-1-ol 
• 244785-05-5 (R,S)-4-hydroxymethyl-imidazolidine-2-thion 
• 87638-26-4 (2R)-2,3-diaminopropan-1-ol 

Relevant articles and documents

Steric effects in the design of Co-Schiff base complexes for the catalytic oxidation of lignin models to para-benzoquinones

New Co-Schiff base complexes that incorporate a sterically hindered ligand and an intramolecular bulky piperazine base in close proximity to the Co center are synthesized. Their utility as catalysts for the oxidation of para-substituted lignin model phenols with molecular oxygen is examined. Syringyl and guaiacyl alcohol, as models of S and G units in lignin, are oxidized in good yield using a catalyst bearing an N-benzylpiperazinyl substituent, with the catalysts displaying improved reactivity for G oxidation. Computational evaluation of the catalysts shows that the piperazinyl substituent is within bonding distance of the Co center. The increased steric interference is suggested as the source of increased G reactivity. This journal is the Partner Organisations 2014.

Tricyclic erythromycin derivatives

Compounds, or pharmaceutically acceptable salts and esters thereof, of the formula: wherein A, B, D and E, R1, R2, and Z are specifically defined, having antibacterial activity, pharmaceutical compositions containing said compounds, treatment of bacterial infections with such compositions, and processes for the preparation of the compounds.