2-Amino-4-propylphenol

Base Information

• Chemical Name: 2-Amino-4-propylphenol
• CAS No.: 55296-63-4
• Molecular Formula: C₉H₁₃NO
• Molecular Weight: 151.208
• European Community (EC) Number: 637-246-9
• Mol file: 55296-63-4.mol

Synonyms:2-amino-4-propylphenol;55296-63-4;TimTec1_000912;Oprea1_506978;SCHEMBL1023135;VXTJVMWIVSZHNI-UHFFFAOYSA-N;HMS1536J10;KUC106773N;STK032250;AKOS000289281;NCGC00174990-01;KSC-11-229-09;BRD-K00938657-001-01-0

Chemical Property of 2-Amino-4-propylphenol

Chemical Property:

• XLogP3: 2.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 151.099714038
• Heavy Atom Count: 11
• Complexity: 116

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CCCC1=CC(=C(C=C1)O)N

Technology Process of 2-Amino-4-propylphenol

There total 7 articles about 2-Amino-4-propylphenol 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:

O-(4-propylphenyl)hydroxylamine → 4-n-Propylphenol (645-56-7) + 2-Amino-4-propyl-phenol (55296-63-4)

Guidance literature:

With trifluoroacetic acid; In dichloromethane; at -15 ℃; for 4h; Product distribution; Rate constant; Kinetics; ΔH(excit.), ΔG(excit.), ΔS(excit.);

DOI:10.1021/ja00051a012

Reference yield:

2-nitro-4-propylphenol (6343-48-2) → 2-Amino-4-propyl-phenol (55296-63-4)

Guidance literature:

With sodium hydroxide; sodium dithionite;

Reference yield:

2-nitro-4-propylphenol (6343-48-2) → 4'-n-propylbenzoxazinorifamycin + 2-Amino-4-propyl-phenol (55296-63-4)

Guidance literature:

With hydrogen; palladium-carbon; In ethanol;

upstream raw materials:

2-nitro-4-propylphenol

4-n-Propylphenol

4-n-propylanisole

methoxybenzene

Downstream raw materials:

acetic acid-(2-hydroxy-5-propyl-anilide)