2-Aminobutane-1,4-diol

Base Information

• Chemical Name: 2-Aminobutane-1,4-diol
• CAS No.: 4426-52-2
• Molecular Formula: C4H11NO2
• Molecular Weight: 105.137
• DSSTox Substance ID: DTXSID40558979

Synonyms:2-aminobutane-1,4-diol;4426-52-2;2-amino-1,4-butanediol;SCHEMBL59325;DTXSID40558979;PYBVXNWDSBYQSA-UHFFFAOYSA-N;MFCD18205986;AKOS006339527;SB46013;SB84511;AS-44403;CS-0091333;EN300-297145

Chemical Property of 2-Aminobutane-1,4-diol

Chemical Property:

• XLogP3: -1.7
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 105.078978594
• Heavy Atom Count: 7
• Complexity: 40.7

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CO)C(CO)N

Technology Process of 2-Aminobutane-1,4-diol

There total 1 articles about 2-Aminobutane-1,4-diol 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:

2-acetamido-1-N-(3-amino-4-hydroxybutyryl)-2-deoxy-β-D-glucopyranosylamine hydrochloride → (2RS)-2-aminobutane-1,4-diol (4426-52-2) + 2-amino-2-deoxy-D-glucitol (14307-03-0,2351-14-6)

Guidance literature:

With hydrogenchloride; lithium borohydride; Yield given. Multistep reaction. Yields of byproduct given; 1.) H₂O, 100 deg C, 16 h, 2.) 40-45 deg C, 1 h;

DOI:10.1007/BF00954837

Reference yield: 53.0%

(2RS)-2-aminobutane-1,4-diol (4426-52-2) + 6-(4-chlorophenyl)-2-(3-fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carboxylic acid → 6-(4-chlorophenyl)-N-[(2RS)-1,4-dihydroxybutan-2-yl]-2-(3-fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide

Guidance literature:

With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield: 24.0%

(2RS)-2-aminobutane-1,4-diol (4426-52-2) + 2-(3-fluorophenyl)-3-oxo-6-[4-(trifluoromethyl)phenyl]-2,3-dihydropyridazine-4-carboxylic acid → N-[(2RS)-1,4-dihydroxybutan-2-yl]-2-(3-fluorophenyl)-3-oxo-6-[4-(trifluoromethyl)phenyl]-2,3-dihydropyridazine-4-carboxamide

Guidance literature:

With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;

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