Antafenite

Base Information

Chemical Name:Antafenite
CAS No.:15301-45-8
Molecular Formula:C₁₁H₁₀N₂S
Molecular Weight:202.28
Hs Code.:
Mol file:15301-45-8.mol

Synonyms:Antafenito;Antafenitum;Antafenite;7-phenyl-4-thia-1,6-diazabicyclo[3.3.0]octa-2,5-diene;R 8193;( -)-5,6-Dihydro-6-phenylimidazo(2,1-b)thiazole;

Suppliers and Price of Antafenite

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
ANTAFENITE 95.00%
5MG
$ 500.62

Total 2 raw suppliers

Chemical Property of Antafenite

Chemical Property:

Vapor Pressure:5.23E-05mmHg at 25°C
Refractive Index:1.712
Boiling Point:347.9°Cat760mmHg
Flash Point:164.2°C
PSA：45.53000
Density:1.31g/cm³
LogP:1.64080

Purity/Quality:

99% ^*data from raw suppliers

ANTAFENITE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Antafenite

There total 6 articles about Antafenite 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: 80.0%

: 10505-59-6
2-(2-imino-thiazol-3-yl)-1-phenyl-ethanol

: 6649-73-6,15301-45-8
dihydro-5,6 phenyl-6 imidazo<2,1-b>thiazole

Guidance literature:: With thionyl chloride; acetic anhydride; at 60 ℃; for 10h;

Reference yield:

: 10505-64-3
2-(2-acetylimino-thiazol-3-yl)-1-phenyl-ethanone

: 6649-73-6,15301-45-8
dihydro-5,6 phenyl-6 imidazo<2,1-b>thiazole

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₄ / propan-2-ol / 1 h / Heating

2: (i) SOCl₂, (ii) Ac₂O

With sodium tetrahydroborate; In isopropyl alcohol;
DOI:10.1021/jm00322a023

Reference yield:

: 116923-07-0
2-amino-3-(2-oxo-2-phenyl-ethyl)-thiazolium; bromide

: 6649-73-6,15301-45-8
dihydro-5,6 phenyl-6 imidazo<2,1-b>thiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / sodium borohydride / methanol

2: 80 percent / acetic anhydride, thionyl chloride / 10 h / 60 °C

With sodium tetrahydroborate; thionyl chloride; acetic anhydride; In methanol;