Opiniazide

Base Information

Chemical Name:Opiniazide
CAS No.:2779-55-7
Molecular Formula:C₁₆H₁₅N₃O₅
Molecular Weight:329.312
Hs Code.:2933399090
UNII:KD4681N5W4
NCI Thesaurus Code:C90770
ChEMBL ID:CHEMBL1403144
Mol file:2779-55-7.mol

Synonyms:1-(2-carboxy-3,4-dimethoxybenzylidene)-2-isonicotinoylhydrazone;opiniazide;saluzid

Suppliers and Price of Opiniazide

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

TRC
Saluzide
50mg
$ 140.00

Aronis compounds
6-(2-isonicotinoylcarbonohydrazonoyl)-2,3-dimethoxybenzoicacid
1g
$ 198.00

American Custom Chemicals Corporation
2,3-DIMETHOXY-6-[(PYRIDINE-4-CARBONYL)-HYDRAZONOMETHYL]-BENZOIC ACID 95.00%
5MG
$ 498.22

Total 5 raw suppliers

Chemical Property of Opiniazide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：110.11000
Density:1.31g/cm³
LogP:1.95180
XLogP3:1.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:6
Exact Mass:329.10117059
Heavy Atom Count:24
Complexity:465

Purity/Quality:

99% ^*data from raw suppliers

Saluzide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C(=C(C=C1)C=NNC(=O)C2=CC=NC=C2)C(=O)O)OC
Isomeric SMILES:COC1=C(C(=C(C=C1)/C=N/NC(=O)C2=CC=NC=C2)C(=O)O)OC
Uses Saluzide is an anti-tuberculosis agent. Also, it is derived from Opianic Acid (O669300), which is a reagent used in the synthesis of novel 5-arylidene (thio)barbituric acid displaying urease activity.

Technology Process of Opiniazide

There total 1 articles about Opiniazide 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: