(2S)-1,4-Diaminobutan-2-ol

Base Information

• Chemical Name: (2S)-1,4-Diaminobutan-2-ol
• CAS No.: 24177-21-7
• Molecular Formula: C4H12N2O
• Molecular Weight: 104.15100
• DSSTox Substance ID: DTXSID20707524
• Nikkaji Number: J88.235F
• Wikidata: Q82641358
• Mol file: 24177-21-7.mol

Synonyms:(2S)-1,4-Diaminobutan-2-ol;24177-21-7;SCHEMBL13745483;DTXSID20707524;S-(+)-2-HO-PUT;EN300-2517144

Chemical Property of (2S)-1,4-Diaminobutan-2-ol

Chemical Property:

• PSA: 72.27000
• LogP: 0.05540
• XLogP3: -1.9
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 104.094963011
• Heavy Atom Count: 7
• Complexity: 40.7

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CN)C(CN)O
• Isomeric SMILES: C(CN)[C@@H](CN)O

Technology Process of (2S)-1,4-Diaminobutan-2-ol

There total 7 articles about (2S)-1,4-Diaminobutan-2-ol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

1,4-diazidobutan-2-ol (145627-47-0) → 2-hydroxybutane-1,4-diamine (539-59-3,24177-21-7)

Guidance literature:

With water; triphenylphosphine; In tetrahydrofuran; at 20 ℃;

Reference yield:

(2S)-malamide (617-47-0) → (S)-1,4-diamino-2-butanol (24177-21-7)

Guidance literature:

With borane-THF; at 77 ℃; for 11h; Inert atmosphere;

DOI:10.1016/j.jcat.2015.12.026

Reference yield:

(2-Benzyl-isoxazolidin-5-ylmethyl)-(2-cyano-ethyl)-carbamic acid benzyl ester (172045-48-6) → 2-hydroxybutane-1,4-diamine (539-59-3,24177-21-7)

Guidance literature:

With hydrogen; palladium on activated charcoal;

DOI:10.1016/0040-4039(95)01976-O

upstream raw materials:

(2-chloro-4-phthalimido-butyl)-carbamic acid ethyl ester

(2-Benzyl-isoxazolidin-5-ylmethyl)-(2-cyano-ethyl)-carbamic acid benzyl ester

1,4-diazidobutan-2-ol

(2S)-malamide

Downstream raw materials:

1,4-bis(salicylideneamino)-2-butanol

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