Benzenemethanamine, N-[2-(phenylseleno)hexyl]-

Base Information

Chemical Name:Benzenemethanamine, N-[2-(phenylseleno)hexyl]-
CAS No.:730907-46-7
Molecular Formula:C19H25NSe
Molecular Weight:346.374
Hs Code.:
DSSTox Substance ID:DTXSID10477603

Synonyms:Benzenemethanamine, N-[2-(phenylseleno)hexyl]-;730907-46-7;WWCGYTWHHNNPAZ-UHFFFAOYSA-;DTXSID10477603;InChI=1/C19H25NSe/c1-2-3-12-19(21-18-13-8-5-9-14-18)16-20-15-17-10-6-4-7-11-17/h4-11,13-14,19-20H,2-3,12,15-16H2,1H3

Suppliers and Price of Benzenemethanamine, N-[2-(phenylseleno)hexyl]-

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

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Chemical Property of Benzenemethanamine, N-[2-(phenylseleno)hexyl]-

Chemical Property:

Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:9
Exact Mass:347.11522
Heavy Atom Count:21
Complexity:244

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCC(CNCC1=CC=CC=C1)[Se]C2=CC=CC=C2

Technology Process of Benzenemethanamine, N-[2-(phenylseleno)hexyl]-

There total 3 articles about Benzenemethanamine, N-[2-(phenylseleno)hexyl]- 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: 65.0%

: 831200-72-7
phenyl-N-(2-(phenylselanyl)hexylidene)methanamine

: 730907-46-7
N-benzyl-2-(phenylselanyl)hexan-1-amine

Guidance literature:: With sodium cyanoborohydride; acetic acid; In ethanol; at -78 ℃; for 1h;
DOI:10.1016/j.tet.2004.10.065

Reference yield:

: 78998-79-5
α-phenylseleno-hexanal

: 730907-46-7
N-benzyl-2-(phenylselanyl)hexan-1-amine

Guidance literature:: Multi-step reaction with 2 steps

1.1: magnesium sulfate / CH₂Cl₂ / 0.17 h / -5 °C

1.2: CH₂Cl₂ / 3 h / 20 °C

2.1: 65 percent / sodium cyanoborohydride; acetic acid / ethanol / 1 h / -78 °C

With sodium cyanoborohydride; magnesium sulfate; acetic acid; In ethanol; dichloromethane;
DOI:10.1016/j.tet.2004.10.065

Reference yield:

: 100-46-9
benzylamine

: 730907-46-7
N-benzyl-2-(phenylselanyl)hexan-1-amine

Guidance literature:: Multi-step reaction with 2 steps

1.1: magnesium sulfate / CH₂Cl₂ / 0.17 h / -5 °C

1.2: CH₂Cl₂ / 3 h / 20 °C

2.1: 65 percent / sodium cyanoborohydride; acetic acid / ethanol / 1 h / -78 °C

With sodium cyanoborohydride; magnesium sulfate; acetic acid; In ethanol; dichloromethane;
DOI:10.1016/j.tet.2004.10.065