Perillartine

Base Information

Chemical Name:Perillartine
CAS No.:138-91-0
Deprecated CAS:28305-56-8,32638-37-2
Molecular Formula:C10H15 N O
Molecular Weight:165.235
Hs Code.:2928000090
European Community (EC) Number:205-344-7,250-402-7
NSC Number:151796,1179
UNII:46S302515I
DSSTox Substance ID:DTXSID701014887
Wikipedia:Perillartine
Metabolomics Workbench ID:47000
ChEMBL ID:CHEMBL21404
Mol file:138-91-0.mol

Synonyms:perillartine;perillartine, (E)-(+)-isomer;perillartine, (E)-(+-)-isomer;perillartine, (E)-(-)-isomer;perillartine, (E)-isomer;perillartine, (S)-isomer

Suppliers and Price of Perillartine

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 11 raw suppliers

Chemical Property of Perillartine

Chemical Property:

Vapor Pressure:0.000845mmHg at 25°C
Melting Point:102°
Boiling Point:271.4°Cat760mmHg
PKA:11.45±0.28(Predicted)
Flash Point:158.3°C
PSA：32.59000
Density:1g/cm³
LogP:2.74900
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:165.115364102
Heavy Atom Count:12
Complexity:228

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=C)C1CCC(=CC1)C=NO
Isomeric SMILES:CC(=C)C1CCC(=CC1)/C=N/O
Uses 4-isopropenylcyclohex-1-enecarbaldehyde oxime is used as sweetening agent in Japan.

Technology Process of Perillartine

There total 4 articles about Perillartine 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: 82.0%

: 536-59-4
perillol

: 138-91-0
p-mentha-1,8-dien-7-al oxime

Guidance literature:: With hydroxylamine hydrochloride; NAD; alcohol dehydrogenase HeADH-II from Halomonas elongata; NADH-oxidase from Lactobacillu spentosus; flavin-adenin dinucleotide, disodium salt; In dimethyl sulfoxide; at 30 ℃; for 2h; pH=8; Enzymatic reaction;
DOI:10.1002/cctc.202001112