Hydroxylamine, O-(1-methylethyl)-

Base Information

• Chemical Name: Hydroxylamine, O-(1-methylethyl)-
• CAS No.: 4427-29-6
• Molecular Formula: C3H9NO
• Molecular Weight: 75.1106
• Hs Code.: 2922199090
• DSSTox Substance ID: DTXSID40196097
• Wikidata: Q83069189
• Mol file: 4427-29-6.mol

Synonyms:Hydroxylamine, O-(1-methylethyl)-;4427-29-6;O-propan-2-ylhydroxylamine;O-(propan-2-yl)hydroxylamine;O-(1-Methylethyl)hydroxylamine;O-isopropylhydroxylamine;isopropoxyamine;O-isopropyl-hydroxylamine;DTXSID40196097;AKOS006283943;EN300-226541

Chemical Property of Hydroxylamine, O-(1-methylethyl)-

Chemical Property:

• Vapor Pressure: 52.2mmHg at 25°C
• Boiling Point: 92.2°Cat760mmHg
• Flash Point: 10.7°C
• PSA: 35.25000
• Density: 0.848g/cm³
• LogP: 0.98540
• XLogP3: 0.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 75.068413911
• Heavy Atom Count: 5
• Complexity: 20.9

Purity/Quality:

95% ^*data from raw suppliers

2-(AMINOOXY)PROPANE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(C)ON

Technology Process of Hydroxylamine, O-(1-methylethyl)-

There total 1 articles about Hydroxylamine, O-(1-methylethyl)- 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:

→ isopropoxyamine (4427-29-6) + anthranilic acid (118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4)

Guidance literature:

Reference yield: 91.0%

isopropoxyamine (4427-29-6) + (Z)-3-acetyl-4-hydroxy-5-(4-methoxybenzylidene)-pyrrolidine-2-one (1262232-42-7) → (Z)-4-hydroxy-3-((E)-1-(isopropoxyimino)ethyl)-5-(4-methoxybenzylidene)-1,5-dihydro-2H-pyrrole-2-one (1262232-56-3)

Guidance literature:

With sodium hydroxide; In ethanol; water; for 3h; Reflux;

DOI:10.1002/jhet.452

Reference yield: 87.2%

isopropoxyamine (4427-29-6) + (Z)-3-acetyl-5-benzylidene-4-hydroxypyrrolidine-2-one → (Z)-5-benzylidene-4-hydroxy-3-((E)-1-(isopropoxyimino)ethyl)-1,5-dihydro-2H-pyrrole-2-one (1262232-47-2)

Guidance literature:

With sodium hydroxide; In ethanol; water; for 3h; Reflux;

DOI:10.1002/jhet.452

Downstream raw materials:

2-(1-Isopropoxyamino-butylidene)-5,5-dimethyl-cyclohexane-1,3-dione

3-Formylrifamycin SV O-i-Propyloxim

O-Isopropyl-phenyl-acetonoxim

3-hydroxy-N-isopropoxy-2,2-diphenyl-propionamide