6-Chloro-3-ethylbenzo[d]thiazol-2(3H)-one

Base Information

Chemical Name:6-Chloro-3-ethylbenzo[d]thiazol-2(3H)-one
CAS No.:30459-51-9
Molecular Formula:C₉H₈ClNOS
Molecular Weight:213.688
Hs Code.:2934200090
European Community (EC) Number:654-377-7
NSC Number:108216
DSSTox Substance ID:DTXSID00296188
Wikidata:Q82036638
Mol file:30459-51-9.mol

Synonyms:6-Chloro-3-ethylbenzo[d]thiazol-2(3H)-one;30459-51-9;6-chloro-3-ethyl-1,3-benzothiazol-2-one;6-chloro-3-ethyl-1,3-benzothiazol-2(3h)-one;NSC108216;2(3H)-Benzothiazolone, 6-chloro-3-ethyl-;6-chloro-3-ethyl-2,3-dihydro-1,3-benzothiazol-2-one;SCHEMBL11038312;DTXSID00296188;AKOS022189272;NSC-108216

Suppliers and Price of 6-Chloro-3-ethylbenzo[d]thiazol-2(3H)-one

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

Crysdot
6-Chloro-3-ethylbenzo[d]thiazol-2(3H)-one 95+%
1g
$ 608.00

Chemenu
6-chloro-3-ethylbenzo[d]thiazol-2(3H)-one 95%
1g
$ 574.00

American Custom Chemicals Corporation
6-CHLORO-3-ETHYL-2-BENZOTHIAZOLINONE 95.00%
5MG
$ 503.95

Total 5 raw suppliers

Chemical Property of 6-Chloro-3-ethylbenzo[d]thiazol-2(3H)-one

Chemical Property:

Vapor Pressure:7.72E-05mmHg at 25°C
Boiling Point:342.1°Cat760mmHg
Flash Point:160.7°C
PSA：50.24000
Density:1.377g/cm³
LogP:2.73630
XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:213.0015127
Heavy Atom Count:13
Complexity:224

Purity/Quality:

≥99% ^*data from raw suppliers

6-Chloro-3-ethylbenzo[d]thiazol-2(3H)-one 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN1C2=C(C=C(C=C2)Cl)SC1=O

Technology Process of 6-Chloro-3-ethylbenzo[d]thiazol-2(3H)-one

There total 4 articles about 6-Chloro-3-ethylbenzo[d]thiazol-2(3H)-one 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:

: 62266-81-3
6-chloro-2,3-dihydrobenzothiazol-2-one

: 30459-51-9
6-Chlor-3-ethylbenzothiazol-2-on

Guidance literature:: With potassium hydroxide;

Reference yield:

: 3622-23-9
2,6-dichloro-1,3-benzothiazole

: 30459-51-9
6-Chlor-3-ethylbenzothiazol-2-on

Guidance literature:: Multi-step reaction with 2 steps

1: aq. HCl

2: KOH

With hydrogenchloride; potassium hydroxide;

Reference yield:

: 95-24-9
6-chloro-2-aminobenzothiazole

: 30459-51-9
6-Chlor-3-ethylbenzothiazol-2-on

Guidance literature:: Multi-step reaction with 3 steps

1: NaNO₂, aq. HCl

2: aq. HCl

3: KOH

With hydrogenchloride; potassium hydroxide; sodium nitrite;