Guanidine, 1-tert-butyl-2-(2-naphthyl)-3-(2-thiazolyl)-

Base Information

Chemical Name:Guanidine, 1-tert-butyl-2-(2-naphthyl)-3-(2-thiazolyl)-
CAS No.:72041-76-0
Molecular Formula:C₁₈H₂₀N₄S
Molecular Weight:324.45
Hs Code.:
DSSTox Substance ID:DTXSID00992734
ChEMBL ID:CHEMBL64733
Mol file:72041-76-0.mol

Synonyms:BRN 5592466;72041-76-0;Guanidine, 1-tert-butyl-2-(2-naphthyl)-3-(2-thiazolyl)-;N-(1,1-Dimethylethyl)-N'-2-naphthalenyl-N''-2-thiazolylguanidine;Guanidine, N-(1,1-dimethylethyl)-N'-2-naphthalenyl-N''-2-thiazolyl-;CHEMBL64733;DTXSID00992734;LS-73602;N-tert-Butyl-N''-naphthalen-2-yl-N'-1,3-thiazol-2-ylguanidine

Suppliers and Price of Guanidine, 1-tert-butyl-2-(2-naphthyl)-3-(2-thiazolyl)-

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
GUANIDINE, 1-TERT-BUTYL-2-(2-NAPHTHYL)-3-(2-THIAZOLYL)- 95.00%
5MG
$ 495.01

Total 3 raw suppliers

Chemical Property of Guanidine, 1-tert-butyl-2-(2-naphthyl)-3-(2-thiazolyl)-

Chemical Property:

Vapor Pressure:3.73E-09mmHg at 25°C
Boiling Point:474.1°C at 760 mmHg
Flash Point:240.5°C
PSA：77.55000
Density:1.18g/cm³
LogP:5.24790
XLogP3:4.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:324.14086783
Heavy Atom Count:23
Complexity:418

Purity/Quality:

99% ^*data from raw suppliers

GUANIDINE, 1-TERT-BUTYL-2-(2-NAPHTHYL)-3-(2-THIAZOLYL)- 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)N=C(NC1=CC2=CC=CC=C2C=C1)NC3=NC=CS3

Technology Process of Guanidine, 1-tert-butyl-2-(2-naphthyl)-3-(2-thiazolyl)-

There total 1 articles about Guanidine, 1-tert-butyl-2-(2-naphthyl)-3-(2-thiazolyl)- 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: 45.0%