N-butyl-4,5-dihydro-1,3-thiazol-2-amine

Base Information

Chemical Name:N-butyl-4,5-dihydro-1,3-thiazol-2-amine
CAS No.:13846-59-8
Molecular Formula:C₇H₁₄N₂S
Molecular Weight:158.268
Hs Code.:2934100090
DSSTox Substance ID:DTXSID40397249
Wikidata:Q82198432
ChEMBL ID:CHEMBL1378743
Mol file:13846-59-8.mol

Synonyms:13846-59-8;N-butyl-4,5-dihydro-1,3-thiazol-2-amine;Butyl-(4,5-dihydro-thiazol-2-yl)-amine;N-Butyl-4,5-dihydrothiazol-2-amine;HMS1723E14;MLS001006355;CHEMBL1378743;DTXSID40397249;HMS2712O23;AKOS000115845;CL-69954;SMR000349337;CS-0219047;EN300-02917;Z56855133

Suppliers and Price of N-butyl-4,5-dihydro-1,3-thiazol-2-amine

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
BUTYL-(4,5-DIHYDRO-THIAZOL-2-YL)-AMINE 95.00%
5G
$ 1005.43

American Custom Chemicals Corporation
BUTYL-(4,5-DIHYDRO-THIAZOL-2-YL)-AMINE 95.00%
2.5G
$ 852.21

American Custom Chemicals Corporation
BUTYL-(4,5-DIHYDRO-THIAZOL-2-YL)-AMINE 95.00%
1G
$ 648.81

Total 3 raw suppliers

Chemical Property of N-butyl-4,5-dihydro-1,3-thiazol-2-amine

Chemical Property:

Vapor Pressure:0.035mmHg at 25°C
Boiling Point:241.9°Cat760mmHg
Flash Point:100.1°C
PSA：49.69000
Density:1.13g/cm³
LogP:1.80770
XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:158.08776963
Heavy Atom Count:10
Complexity:123

Purity/Quality:

97% ^*data from raw suppliers

BUTYL-(4,5-DIHYDRO-THIAZOL-2-YL)-AMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCNC1=NCCS1

Technology Process of N-butyl-4,5-dihydro-1,3-thiazol-2-amine

There total 4 articles about N-butyl-4,5-dihydro-1,3-thiazol-2-amine 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: 35.0%

: 27803-70-9
1-Butyl-3-(2-hydroxy-ethyl)-thiourea

: 13846-59-8
2-Butylamino-thiazolin

Guidance literature:: With hydrogenchloride;

Reference yield:

: phosphoric acid mono-[2-(3-butyl-thioureido)-ethyl] ester; disodium salt

: 13846-59-8
2-Butylamino-thiazolin

Guidance literature:: With ion-exchange resin + form>; In water; Ambient temperature;

Reference yield:

: 592-82-5
butyl isothiocyanate

: 13846-59-8
2-Butylamino-thiazolin

Guidance literature:: Multi-step reaction with 2 steps

1: 50 percent / toluene / Ambient temperature

2: 35 percent / conc. HCl

With hydrogenchloride; In toluene;