1-Isonicotinyl-2-palmitoyl hydrazine

Base Information

Chemical Name:1-Isonicotinyl-2-palmitoyl hydrazine
CAS No.:101524-04-3
Molecular Formula:C₂₂H₃₇N₃O₂
Molecular Weight:375.555
Hs Code.:
DSSTox Substance ID:DTXSID00906295
Nikkaji Number:J371.910C
Wikidata:Q82874996
ChEMBL ID:CHEMBL2443180
Mol file:101524-04-3.mol

Synonyms:1-isonicotinyl-2-palmitoyl hydrazine;INH-PALM

Suppliers and Price of 1-Isonicotinyl-2-palmitoyl hydrazine

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 1 raw suppliers

Chemical Property of 1-Isonicotinyl-2-palmitoyl hydrazine

Chemical Property:

Vapor Pressure:1.09E-12mmHg at 25°C
Boiling Point:562.7°C at 760 mmHg
Flash Point:294.1°C
PSA：71.09000
Density:0.997g/cm³
LogP:6.10570
XLogP3:7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:15
Exact Mass:375.28857743
Heavy Atom Count:27
Complexity:382

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCC(=O)NNC(=O)C1=CC=NC=C1

Technology Process of 1-Isonicotinyl-2-palmitoyl hydrazine

There total 3 articles about 1-Isonicotinyl-2-palmitoyl hydrazine 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:

: 54-85-3,7640-37-1
isoniazid

: 112-67-4
n-hexadecanoyl chloride

: 101524-04-3
N′-hexadecanoylisonicotinohydrazide

Guidance literature:: With 1,4-dioxane; pyridine;
DOI:10.1021/jo50016a018

Reference yield:

: 57-10-3
1-hexadecylcarboxylic acid

: 101524-04-3
N′-hexadecanoylisonicotinohydrazide

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl dichloride / dichloromethane / 0.5 h / 20 °C

2: dmap / dichloromethane / 12 h / 20 °C

With dmap; oxalyl dichloride; In dichloromethane;
DOI:10.1016/j.bmc.2013.09.034