5-Amino-2,2-dimethylpentanol

Base Information

• Chemical Name: 5-Amino-2,2-dimethylpentanol
• CAS No.: 13532-77-9
• Molecular Formula: C7H17NO
• Molecular Weight: 131.218
• Hs Code.: 2922199090
• European Community (EC) Number: 627-210-0
• DSSTox Substance ID: DTXSID70159312
• Nikkaji Number: J2.453.370K
• Wikidata: Q83027616
• Mol file: 13532-77-9.mol

Synonyms:5-Amino-2,2-dimethylpentanol;13532-77-9;5-amino-2,2-dimethylpentan-1-ol;5-Amino-2,2-dimethyl-pentan-1-ol;2,2-Dimethyl-5-amino-1-pentanol;5-Amino-2,2-dimethyl-1-pentanol;1-Pentanol, 5-amino-2,2-dimethyl-;SCHEMBL994485;DTXSID70159312;5-amino-2,2,-dimethylpentan-1-ol;MFCD00043626;5-Amino-2,2-dimethyl-1-pentanol #;AKOS000303030;SB83883;BS-23320;CS-0119951;FT-0619971;EN300-84776;J-006682;Z1203160200

Chemical Property of 5-Amino-2,2-dimethylpentanol

Chemical Property:

• Vapor Pressure: 0.00706mmHg at 25°C
• Boiling Point: 239.4 °C at 760 mmHg
• PKA: 15.19±0.10(Predicted)
• Flash Point: 98.6 °C
• PSA: 46.25000
• Density: 0.903 g/cm³
• LogP: 1.44410
• XLogP3: 0.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 131.131014166
• Heavy Atom Count: 9
• Complexity: 71.3

Purity/Quality:

98%,99%, ^*data from raw suppliers

5-Amino-2,2-dimethylpentan-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn,Xi
• Hazard Codes: Xn,Xi
• Statements: 22-36-43
• Safety Statements: 26-37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(CCCN)CO
• Uses: Reactant for:Reductive amination with borohydride and borane reducing agentsCopper-catalyzed N- and O-arylation with aryl iodidesPreparation of N-(alkyl)arylamine derivatives via selective room-temperature carbon-nitrogen coupling reaction using copper iodide as catalyst and diketone as ligand

Technology Process of 5-Amino-2,2-dimethylpentanol

There total 1 articles about 5-Amino-2,2-dimethylpentanol 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:

4,4-dimethyl-5-hydroxyvaleronitrile (25252-68-0) → 5-amino-2,2-dimethylpentan-1-ol (13532-77-9)

Guidance literature:

With ammonia; hydrogen; nickel; In ethanol;

Reference yield: 100.0%

5-amino-2,2-dimethylpentan-1-ol (13532-77-9) + (4-isocyanatobutyl)benzene (77725-08-7) → N-(5-hydroxy-4,4-dimethylpentyl)-N'-(4-phenylbutyl)urea

Guidance literature:

In dichloromethane; Column chromatography;

Reference yield: 100.0%

5-amino-2,2-dimethylpentan-1-ol (13532-77-9) + 3-phenylpropylisocyanate (68664-23-3) → N-(5-hydroxy-4,4-dimethylpentyl)-N'-(3-phenylpropyl)urea

Guidance literature:

In dichloromethane; Column chromatography;

upstream raw materials:

4,4-dimethyl-5-hydroxyvaleronitrile

Downstream raw materials:

3-(4-fluoro-phenyl)-1,5-diphenyl-4,5-dihydro-1H-pyrazole-4-carboxylic acid (5-hydroxy-4,4-dimethyl-pentyl)-amide

1,3-diphenyl-(5-thiophen-3-yl)-4,5-dihydro-1H-pyrazole-4-carboxylic acid (5-hydroxy-4,4-dimethylpentyl)amide