(E)-Alprenoxime

Base Information

Chemical Name:(E)-Alprenoxime
CAS No.:125720-84-5
Molecular Formula:C15H22N2O2
Molecular Weight:262.34700
Hs Code.:
UNII:ZH6X5L4LHF
Nikkaji Number:J397.311E
ChEMBL ID:CHEMBL2105963
Mol file:125720-84-5.mol

Synonyms:(E)-Alprenoxime;125720-84-5;(NE)-N-[1-(propan-2-ylamino)-3-(2-prop-2-enylphenoxy)propan-2-ylidene]hydroxylamine;(Z)-Alprenoxime;CDDD-1815;Alprenoxime, (E)-;ZH6X5L4LHF;D0D5DE;SCHEMBL1255825;SCHEMBL9817961;CHEMBL2105963;Alprenoxime hydrochloride < USAN >;AKOS040732214;CS-6581;HY-101804;L003903;1-(2-Allylphenoxy)-3-(isopropylamino)-2-propanone oxime monohydrochloride;1-[(1-Methylethyl)amino]-3-[2-(2-propen-1-yl)phenoxy]-2-propanone oxime;1-[(1-Methylethyl)amino]-3-[2-(2-propenyl)phenoxy]-2-propanone oxime monohydrochloride;2-Propanone, 1-[(1-methylethyl)amino]-3-[2-(2-propen-1-yl)phenoxy]-, oxime;2-Propanone, 1-[(1-methylethyl)amino]-3-[2-(2-propenyl)phenoxy]-, oxime, (E)-

Suppliers and Price of (E)-Alprenoxime

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

Total 3 raw suppliers

Chemical Property of (E)-Alprenoxime

Chemical Property:

Boiling Point:398.7±37.0 °C(Predicted)
PKA:11.41±0.10(Predicted)
PSA：53.85000
Density:1.02±0.1 g/cm3(Predicted)
LogP:3.01300
XLogP3:3.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:8
Exact Mass:262.168127949
Heavy Atom Count:19
Complexity:290

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)NCC(=NO)COC1=CC=CC=C1CC=C
Isomeric SMILES:CC(C)NC/C(=N\O)/COC1=CC=CC=C1CC=C

Technology Process of (E)-Alprenoxime

There total 2 articles about (E)-Alprenoxime 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:

: 13707-88-5
alprenolol hydrochloride

: 125721-08-6
3-(2-Allyl-phenoxy)-2-[(Z)-hydroxyimino]-propionaldehyde oxime

: 125720-99-2
3-(2-Allyl-phenoxy)-2-[(E)-hydroxyimino]-propionaldehyde oxime

: 125720-60-7
1-(2-Allyl-phenoxy)-3-isopropylamino-propan-2-one oxime

: 125720-84-5
1-(2-Allyl-phenoxy)-3-isopropylamino-propan-2-one oxime

Guidance literature:: With oxalyl dichloride; hydroxylamine hydrochloride; dimethyl sulfoxide; triethylamine; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given; 1.) CH₂Cl₂, -60 to -40 deg C, 2.) CH₂Cl₂, -40 to -25 deg C, 3.) CH₂Cl₂, H₂O, EtOH, RT,;
DOI:10.1016/S0040-4020(01)81305-3