Z-3-Amino-propenal

Base Information

• Chemical Name: Z-3-Amino-propenal
• CAS No.: 25186-34-9
• Molecular Formula: C3H5NO
• Molecular Weight: 71.0788
• DSSTox Substance ID: DTXSID60515145,DTXSID901313768
• Nikkaji Number: J765.537A
• Wikidata: Q72441229
• Mol file: 25186-34-9.mol

Synonyms:Z-3-Amino-propenal;(Z)-3-aminoprop-2-enal;25186-34-9;3-Aminoacrolein;(Z)-3-aminoacrylaldehyde;(z)-3-amino-2-propenal;(2Z)-3-Aminoprop-2-enal;76063-24-6;(Z)-3-Amino-propenal;1-Propen-1-ol, 3-imino-;DTXSID60515145;DTXSID901313768;55135-67-6

Chemical Property of Z-3-Amino-propenal

Chemical Property:

• Melting Point: 104-105℃
• Boiling Point: 295℃
• PKA: 5.50±0.70(Predicted)
• Flash Point: 132℃
• PSA: 43.09000
• Density: 0.978
• LogP: 0.35800
• XLogP3: -0.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 71.037113783
• Heavy Atom Count: 5
• Complexity: 48.9

Purity/Quality:

97% ^*data from raw suppliers

Z-3-Amino-propenal ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(=CN)C=O
• Isomeric SMILES: C(=C\N)\C=O

Technology Process of Z-3-Amino-propenal

There total 5 articles about Z-3-Amino-propenal 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: 100.0%

ISOXAZOLE (288-14-2) → 3-aminoprop-2-enal (25186-34-9)

Guidance literature:

With hydrogen; nickel; In methanol; at 20 ℃; under 2068.65 Torr;

Reference yield: 60.0%

Propargylic aldehyde (624-67-9) → 3-aminoprop-2-enal (25186-34-9)

Guidance literature:

With N-methylcyclohexylamine; ammonia; In ethanol; benzene; at 35 ℃; for 1h;

DOI:10.1007/BF00474354

Reference yield:

malondialdehyde (927-76-4) → 3-aminoprop-2-enal (25186-34-9)

Guidance literature:

With ammonia;

DOI:10.1007/BF00938366

upstream raw materials:

ISOXAZOLE

Propargylic aldehyde

malondialdehyde

3-ethoxyacrolein

Downstream raw materials:

6-benzyloxycarbonylamino-5,6,7,8-tetrahydroquinoline

6-benzyl-5,6,7,8-tetrahydro-1,6-naphthyridine

2,3-cycloheptenopyridine

5,6,7,8,9,10,11,12,13,14-decahydrocyclododecapyridine