N-Benzyl-2-methylbut-3-en-2-amine

Base Information

Chemical Name:N-Benzyl-2-methylbut-3-en-2-amine
CAS No.:104937-87-3
Molecular Formula:C12H17N
Molecular Weight:175.274
Hs Code.:
DSSTox Substance ID:DTXSID20543560
Nikkaji Number:J1.748.452D
Wikidata:Q82420479
Mol file:104937-87-3.mol

Synonyms:104937-87-3;N-Benzyl-2-methylbut-3-en-2-amine;SCHEMBL11811445;DTXSID20543560

Suppliers and Price of N-Benzyl-2-methylbut-3-en-2-amine

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-Benzyl-2-methylbut-3-en-2-amine

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:175.136099547
Heavy Atom Count:13
Complexity:155

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C=C)NCC1=CC=CC=C1

Technology Process of N-Benzyl-2-methylbut-3-en-2-amine

There total 16 articles about N-Benzyl-2-methylbut-3-en-2-amine 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%

: 217189-21-4
N-benzyl-N-(1,1-dimethylallyl)hydroxylamine

: 104937-87-3
N-benzyl-α,α-dimethylallylamine

Guidance literature:: With hydrogenchloride; zinc; at 80 ℃; for 1h;
DOI:10.1039/b205323n

Reference yield: 90.0%

: 1191-16-8
3-methylbut-2-enyl acetate

: 100-46-9
benzylamine

: 104937-87-3
N-benzyl-α,α-dimethylallylamine

: 61907-84-4
N-benzyl-N-(3-methyl-2-buten-1-yl) amine

Guidance literature:: With bis(η3-allyl-μ-chloropalladium(II)); 1,8-diazabicyclo[5.4.0]undec-7-ene; triethyl phosphite; In tetrahydrofuran; at 20 ℃; for 20h; regioselective reaction; Inert atmosphere;
DOI:10.1021/jo3025253

Reference yield: 54.0%

: 116504-03-1
prenyl ethyl carbonate

: 100-46-9
benzylamine

: 104937-87-3
N-benzyl-α,α-dimethylallylamine

Guidance literature:: With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triphenylphosphine; In acetonitrile; Heating;
DOI:10.1016/j.tet.2005.01.048