Zinviroxime

Base Information

Chemical Name:Zinviroxime
CAS No.:72301-78-1
Molecular Formula:C₁₇H₁₈N₄O₃S
Molecular Weight:358.421
Hs Code.:
UNII:9SWB3P2O2S
DSSTox Substance ID:DTXSID101024511
Nikkaji Number:J18.804B,J22.664E
Wikidata:Q27251466
NCI Thesaurus Code:C95289
ChEMBL ID:CHEMBL121883
Mol file:72301-78-1.mol

Synonyms:(E)-2-Amino-6-benzoyl-1-(isopropylsulfonyl)benzimidazole oxime;(Z)-2-Amino-6-benzoyl-1-(isopropylsulfonyl)benzimidazole oxime;2-amino-1-(isopropylsulfonyl)-6-benzimidazole phenyl ketone oxime;2-amino-6-benzoyl-1-(isopropylsulfonyl)benzimidazole oxime;6-(((hydroxyimino)phenyl)methyl)-1-((1-methylethyl)sulfonyl)-1H-benzimidazol-2-amine;AR 336;AR-336;enviroxime;Lilly 122771-72;Lilly 122772;LY 122771-72;LY 122772;viroxime;zinviroxime

Suppliers and Price of Zinviroxime

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

Medical Isotopes, Inc.
Zinviroxime
10 mg
$ 650.00

Total 3 raw suppliers

Chemical Property of Zinviroxime

Chemical Property:

Vapor Pressure:1.35E-15mmHg at 25°C
Boiling Point:607.2°C at 760 mmHg
Flash Point:321°C
PSA：119.68000
Density:1.41g/cm³
LogP:3.44230
XLogP3:3.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:358.10996162
Heavy Atom Count:25
Complexity:596

Purity/Quality:

99% ^*data from raw suppliers

Zinviroxime ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)S(=O)(=O)N1C2=C(C=CC(=C2)C(=NO)C3=CC=CC=C3)N=C1N
Isomeric SMILES:CC(C)S(=O)(=O)N1C2=C(C=CC(=C2)/C(=N\O)/C3=CC=CC=C3)N=C1N
Uses Zinviroxime is the (Z)-isomer of Enviroxime Zinviroxime is the (Z)-isomer of Enviroxime (E559600). Zinviroxime is a benzimidazole derivative that inhibits rhinovirus multiplication.

Technology Process of Zinviroxime

There total 3 articles about Zinviroxime 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: 98.0%

: 63198-97-0,72301-78-1,72301-79-2
enviroxime

Guidance literature:

Reference yield:

: 63197-61-5
1-isopropylsulfonyl-2-amino-6-benzoylbenzimidazole

: 72301-78-1
syn-6-<<(hydroxyimino)phenyl>methyl>-1-<(1-methylethyl)sulfonyl>-1H-benzimidazol-2-amine

: 63198-97-0,72301-78-1,72301-79-2
enviroxime

Guidance literature:: With hydroxylamine hydrochloride; In methanol; for 24h; Yield given. Yields of byproduct given; Heating;
DOI:10.1021/jm00178a004

Reference yield:

: 63197-61-5
1-isopropylsulfonyl-2-amino-6-benzoylbenzimidazole

: 72301-78-1
syn-6-<<(hydroxyimino)phenyl>methyl>-1-<(1-methylethyl)sulfonyl>-1H-benzimidazol-2-amine

: 63198-97-0,72301-78-1,72301-79-2
enviroxime

Guidance literature:: With hydroxylamine hydrochloride; In methanol; for 24h; Yield given. Yields of byproduct given; Heating;
DOI:10.1021/jm00178a004