Lupitidine

Base Information

Chemical Name:Lupitidine
CAS No.:83903-06-4
Molecular Formula:C₂₁H₂₇N₅O₂S
Molecular Weight:413.544
Hs Code.:
UNII:WF028DWK9N
DSSTox Substance ID:DTXSID5043760
Nikkaji Number:J33.141D
Wikipedia:Lupitidine
NCI Thesaurus Code:C170142
ChEMBL ID:CHEMBL69178
Mol file:83903-06-4.mol

Synonyms:lupitidine

Suppliers and Price of Lupitidine

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

American Custom Chemicals Corporation
LUPITIDINE 95.00%
5MG
$ 496.02

Total 4 raw suppliers

Chemical Property of Lupitidine

Chemical Property:

Vapor Pressure:1.52E-12mmHg at 25°C
Boiling Point:559.4°C at 760 mmHg
Flash Point:292.1°C
PSA：112.35000
Density:1.25g/cm³
LogP:3.13700
XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:10
Exact Mass:413.18854629
Heavy Atom Count:29
Complexity:610

Purity/Quality:

95% ^*data from raw suppliers

LUPITIDINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NC=C(C=C1)CC2=CN=C(NC2=O)NCCSCC3=CC=C(O3)CN(C)C
Uses Antagonist (to histamine H2receptors, veterinary).

Technology Process of Lupitidine

There total 6 articles about Lupitidine 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:

: 36415-21-1
2-[[[2-furanyl]methyl]thio]ethanamine

: 83903-06-4
Lupitidine

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / ethanol / 24 h / Heating

2: H₂O; acetic acid / Heating

In ethanol; water; acetic acid;
DOI:10.1016/0223-5234(90)90204-G

Reference yield:

: 72716-93-9
2-nitroamino-5-(6-methylpyrid-3-ylmethyl)-4(1H)-pyrimidone

: 83903-06-4
Lupitidine

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / ethanol / 24 h / Heating

2: H₂O; acetic acid / Heating

In ethanol; water; acetic acid;
DOI:10.1016/0223-5234(90)90204-G