Isonicotinic acid, cinnamylidenehydrazide

Base Information

Chemical Name:Isonicotinic acid, cinnamylidenehydrazide
CAS No.:4813-11-0
Molecular Formula:C15H13N3O
Molecular Weight:251.288
Hs Code.:
European Community (EC) Number:225-382-8
NSC Number:33763
ChEMBL ID:CHEMBL3198390
Mol file:4813-11-0.mol

Synonyms:EINECS 225-382-8;ISONICOTINIC ACID, CINNAMYLIDENEHYDRAZIDE;NSC 33763;4813-11-0;BRN 0191043;1'(Or 2')-(cinnamylidene)isonicotinohydrazide;Isonicotinic acid (3-phenyl-allylidene)-hydrazide;NSC33763;4-Pyridinecarboxylic acid, (3-phenyl-2-propenylidene)hydrazide;4-22-00-00575 (Beilstein Handbook Reference);N'-(3-Phenyl-2-propen-1-ylidene)isonicotinohydrazide;N'-[(1E,2E)-3-phenylprop-2-en-1-ylidene]pyridine-4-carbohydrazide;Pyromucic acid, hydrazide;MLS000566438;SCHEMBL2999202;CHEMBL3198390;HMS1609O02;Cinnamaldehyde isonicotinoyl hydrazone;N-[(E)-[(E)-3-phenylprop-2-enylidene]amino]pyridine-4-carboxamide;NSC-33763;STK166266;AKOS000715090;NCGC00245254-01;LS-84874;SMR000176598;N'-((e)-3-phenylallylidene)isonicotinohydrazide

Suppliers and Price of Isonicotinic acid, cinnamylidenehydrazide

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 5 raw suppliers

Chemical Property of Isonicotinic acid, cinnamylidenehydrazide

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:251.105862047
Heavy Atom Count:19
Complexity:326

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=CC=NNC(=O)C2=CC=NC=C2
Isomeric SMILES:C1=CC=C(C=C1)/C=C/C=N/NC(=O)C2=CC=NC=C2

Technology Process of Isonicotinic acid, cinnamylidenehydrazide

There total 4 articles about Isonicotinic acid, cinnamylidenehydrazide 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: 76.0%