Benzenamine, N-hydroxy-N-2-propenyl-

Base Information

Chemical Name:Benzenamine, N-hydroxy-N-2-propenyl-
CAS No.:117531-28-9
Molecular Formula:C9H11NO
Molecular Weight:149.192
Hs Code.:
DSSTox Substance ID:DTXSID90438813
Wikidata:Q82254644
Mol file:117531-28-9.mol

Synonyms:Benzenamine, N-hydroxy-N-2-propenyl-;117531-28-9;N-phenyl-N-prop-2-enylhydroxylamine;N-allyl-N-phenylhydroxylamine;SCHEMBL377078;DTXSID90438813

Suppliers and Price of Benzenamine, N-hydroxy-N-2-propenyl-

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of Benzenamine, N-hydroxy-N-2-propenyl-

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:149.084063974
Heavy Atom Count:11
Complexity:119

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCN(C1=CC=CC=C1)O

Technology Process of Benzenamine, N-hydroxy-N-2-propenyl-

There total 4 articles about Benzenamine, N-hydroxy-N-2-propenyl- 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: 91.0%

: 591-87-7
Allyl acetate

: 100-65-2
N-Phenylhydroxylamine

: 117531-28-9
N-allyl-N-(phenyl)hydroxylamine

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran;
DOI:10.1016/0040-4039(88)85061-5

Reference yield: 29.0%

: 2622-05-1
allylmagnesium bromide

: 586-96-9
Nitrosobenzene

: 117531-28-9
N-allyl-N-(phenyl)hydroxylamine

: 1227476-15-4
Azobenzene

: 495-48-7,55599-32-1
azoxybenzene

Guidance literature:: In tetrahydrofuran; at -70 ℃; for 20h;

Reference yield:

: 688-61-9,53588-88-8,90721-85-0,151452-33-4,151452-35-6
Triallylborane

: 586-96-9
Nitrosobenzene

: 117531-28-9
N-allyl-N-(phenyl)hydroxylamine

: 558484-57-4
O-allyl-N-phenylhydroxylamine

Guidance literature:: Triallylborane; Nitrosobenzene; In tetrahydrofuran; at -65 - 20 ℃; for 2h;

With triethanolamine; In tetrahydrofuran;
DOI:10.1070/mc2002v012n05abeh001640