N-Benzylidene-3,4-(methylenedioxy)benzylamine

Base Information

Chemical Name:N-Benzylidene-3,4-(methylenedioxy)benzylamine
CAS No.:112776-37-1
Molecular Formula:C15H13 N O2
Molecular Weight:239.274
Hs Code.:
DSSTox Substance ID:DTXSID70399973
Mol file:112776-37-1.mol

Synonyms:N-Benzylidene-3,4-(methylenedioxy)benzylamine;112776-37-1;N-(1,3-benzodioxol-5-ylmethyl)-1-phenylmethanimine;130517-95-2;N-benzylidene-piperonylamine;DTXSID70399973;AKOS003267135;FT-0752760

Suppliers and Price of N-Benzylidene-3,4-(methylenedioxy)benzylamine

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

Sigma-Aldrich
N-(3,4-Methylenedioxybenzylidene)benzylamine
1 g
$ 59.10

Alfa Aesar
N-Benzylidene-3,4-(methylenedioxy)benzylamine, 98+%
25g
$ 527.00

Alfa Aesar
N-Benzylidene-3,4-(methylenedioxy)benzylamine, 98+%
5g
$ 145.00

Alfa Aesar
N-Benzylidene-3,4-(methylenedioxy)benzylamine, 98+%
1g
$ 39.80

Total 8 raw suppliers

Chemical Property of N-Benzylidene-3,4-(methylenedioxy)benzylamine

Chemical Property:

Vapor Pressure:0.00124mmHg at 25°C
Melting Point:69.5-70 °C(lit.)
Boiling Point:308.4°Cat760mmHg
PKA:4.45±0.50(Predicted)
Flash Point:140.3°C
PSA：30.82000
Density:g/cm³
LogP:3.03440
XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:239.094628657
Heavy Atom Count:18
Complexity:286

Purity/Quality:

98%min ^*data from raw suppliers

N-(3,4-Methylenedioxybenzylidene)benzylamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:T,N
Statements: 25-37/38-41-51/53
Safety Statements: 26-36/37/39-45-61

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1OC2=C(O1)C=C(C=C2)CN=CC3=CC=CC=C3

Technology Process of N-Benzylidene-3,4-(methylenedioxy)benzylamine

There total 4 articles about N-Benzylidene-3,4-(methylenedioxy)benzylamine 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%