N-Cyclopropylaniline

Base Information

Chemical Name:N-Cyclopropylaniline
CAS No.:34535-98-3
Molecular Formula:C9H11N
Molecular Weight:133.193
Hs Code.:2921420090
European Community (EC) Number:829-311-7
DSSTox Substance ID:DTXSID50426812
Nikkaji Number:J1.483.019G
Wikidata:Q82239619
Mol file:34535-98-3.mol

Synonyms:N-Cyclopropylaniline;34535-98-3;MFCD04038984;Benzenamine, N-cyclopropyl-;phenylcyclopropylamine;N-cyclopropyl aniline;cyclopropyl-phenyl-amine;SCHEMBL236978;DTXSID50426812;AOTWIFLKURJQGE-UHFFFAOYSA-N;AKOS006223716;BS-16632;SY207735;CS-0187583;FT-0732967;D82826;EN300-247487;Z1203731288

Suppliers and Price of N-Cyclopropylaniline

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
N-cyclopropylaniline
10mg
$ 65.00

Crysdot
N-Cyclopropylaniline 95+%
1g
$ 339.00

Chemenu
N-cyclopropylaniline 95%
1g
$ 320.00

Alichem
N-Cyclopropylaniline
1g
$ 400.00

AK Scientific
Phenylcyclopropylamine
250mg
$ 417.00

Acrotein
N-Cyclopropylaniline 97%
0.5g
$ 256.67

Total 8 raw suppliers

Chemical Property of N-Cyclopropylaniline

Chemical Property:

PSA：12.03000
LogP:2.33390
Storage Temp.:2-8°C(protect from light)
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:133.089149355
Heavy Atom Count:10
Complexity:101

Purity/Quality:

99% ^*data from raw suppliers

N-cyclopropylaniline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC1NC2=CC=CC=C2

Technology Process of N-Cyclopropylaniline

There total 14 articles about N-Cyclopropylaniline 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: 92.0%

: 108-86-1,52753-63-6
bromobenzene

: 765-30-0
Cyclopropylamine

: 34535-98-3
D,L-cis-phenylcyclopropylamine

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; dicyclohexyl[3,6-dimethoxy-2′,4′,6′-tris(1-methylethyl)[1,1′-biphenyl]-2-yl]phosphine; sodium tert-pentoxide; In toluene; at 80 ℃; for 18h; Inert atmosphere; Glovebox;
DOI:10.1002/adsc.201400742

Reference yield: 72.0%

: 321532-64-3
N-cyclopropyl-2-phenoxyacetamide

: 34535-98-3
D,L-cis-phenylcyclopropylamine

Guidance literature:: With potassium hydroxide; In 1-methyl-pyrrolidin-2-one; toluene; at 120 - 130 ℃;
DOI:10.1055/s-0032-1318389

Reference yield: 62.0%

: 400777-68-6
N-benzyl-N-cyclopropyl-N-phenylamine

: 34535-98-3
D,L-cis-phenylcyclopropylamine

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; acetic acid; for 4h; under 3000.3 Torr;
DOI:10.1002/1099-0690(200110)2001:20<3811::AID-EJOC3811>3.0.CO;2-6