4-(Allyloxy)aniline

Base Information

• Chemical Name: 4-(Allyloxy)aniline
• CAS No.: 1688-69-3
• Molecular Formula: C9H11NO
• Molecular Weight: 149.192
• Hs Code.: 2922299090
• DSSTox Substance ID: DTXSID20424704
• Nikkaji Number: J1.108.641A
• Wikidata: Q82237383
• Mol file: 1688-69-3.mol

Synonyms:4-(allyloxy)aniline;1688-69-3;4-prop-2-enoxyaniline;p-allyloxyaniline;(4-allyloxy-phenyl)-amine;SCHEMBL717196;4-(prop-2-en-1-yloxy)aniline;DTXSID20424704;HVOANTMNYBSIGH-UHFFFAOYSA-N;3-[(4-Amino)phenoxy]-1-propene;BAA68869;MFCD01902260;STL066415;AKOS000104825;BS-35771;AM20030126;CS-0315119;FT-0720164

Chemical Property of 4-(Allyloxy)aniline

Chemical Property:

• Vapor Pressure: 0.00642mmHg at 25°C
• Boiling Point: 271.5oC at 760 mmHg
• Flash Point: 126.7oC
• PSA: 35.25000
• Density: 1.037g/cm3
• LogP: 2.41480
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 149.084063974
• Heavy Atom Count: 11
• Complexity: 117

Purity/Quality:

98%Min ^*data from raw suppliers

4-(allyloxy)aniline ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CCOC1=CC=C(C=C1)N

Technology Process of 4-(Allyloxy)aniline

There total 25 articles about 4-(Allyloxy)aniline 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%

1-allyloxy-4-nitrobenzene (1568-66-7) → p-allyloxyaniline (1688-69-3)

Guidance literature:

With hydrazine hydrate; In ethanol; at 20 ℃; for 4h; chemoselective reaction;

DOI:10.1021/acscatal.5b00830

Reference yield: 98.0%

1-allyloxy-4-azido-benzene → p-allyloxyaniline (1688-69-3)

Guidance literature:

With hydrazine hydrate; In ethanol; at 20 ℃; chemoselective reaction;

DOI:10.1021/acscatal.6b01217

Reference yield: 93.2%

1-allyloxy-4-nitrobenzene (1568-66-7) + 1-nitro-4-(prop-2-ynyloxy)benzene (17061-85-7) → p-allyloxyaniline (1688-69-3)

Guidance literature:

upstream raw materials:

1-allyloxy-4-nitrobenzene

4-acetamidophenyl allyl ether

allyl-(4-allyloxyphenyl)-amine

4-amino-phenol

Downstream raw materials:

1-isocyanato-4-(allyloxy)benzene

4-allyloxy-N,N-dimethyl-aniline

3-(2-hydroxy-5-aminophenyl)-1-propene

4-acetamidophenyl allyl ether