3-Oxo-1,2-benzisothiazole-2(3H)-acetamide

Base Information

Chemical Name:3-Oxo-1,2-benzisothiazole-2(3H)-acetamide
CAS No.:64552-26-7
Molecular Formula:C9H8 N2 O2 S
Molecular Weight:208.241
Hs Code.:2934999090
European Community (EC) Number:264-941-0
UNII:8GGH6W65A8
DSSTox Substance ID:DTXSID50983177
Nikkaji Number:J307.251G
Wikidata:Q82970081

Synonyms:64552-26-7;3-Oxo-1,2-benzisothiazole-2(3H)-acetamide;EINECS 264-941-0;2-(3-Oxo-1,2-benzisothiazolin-2-yl)-acetamide;3-Oxo-1,2-benzisothiazole-2(3H)acetamide;1,2-Benzisothiazole-2(3H)-acetamide, 3-oxo-;2-(3-oxobenzo[d]isothiazol-2(3H)-yl)acetamide;8GGH6W65A8;2-(3-oxo-2,3-dihydro-1,2-benzothiazol-2-yl)acetamide;SCHEMBL12205847;DTXSID50983177;DWVOOOVGVIEHIA-UHFFFAOYSA-N;NS00053147;2-(3-Oxo-1,2-benzothiazol-2(3H)-yl)ethanimidic acid

Suppliers and Price of 3-Oxo-1,2-benzisothiazole-2(3H)-acetamide

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

Total 4 raw suppliers

Chemical Property of 3-Oxo-1,2-benzisothiazole-2(3H)-acetamide

Chemical Property:

Vapor Pressure:5.35E-09mmHg at 25°C
Boiling Point:469.8°C at 760 mmHg
Flash Point:237.9°C
PSA：94.32000
Density:1.446g/cm³
LogP:1.69800
XLogP3:0.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:208.03064868
Heavy Atom Count:14
Complexity:270

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=O)N(S2)CC(=O)N

Technology Process of 3-Oxo-1,2-benzisothiazole-2(3H)-acetamide

There total 2 articles about 3-Oxo-1,2-benzisothiazole-2(3H)-acetamide 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: 64.0%

: 4299-16-5
(1,2-Benzisothiazolin-3-on-2-yl)essigsaeureethylester

: 64552-26-7
(1,2-Benzoisothiazolin-3-on-2-yl)essigsaeureamid

Guidance literature:: With ammonium hydroxide; for 24h; Ambient temperature;

Reference yield:

: 2634-33-5
1,2-benzisothiazolin-3-one

: 64552-26-7
(1,2-Benzoisothiazolin-3-on-2-yl)essigsaeureamid

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / triethylamine / benzene / 24 h / Ambient temperature

2: 64 percent / 25percent NH₃ / 24 h / Ambient temperature

With ammonium hydroxide; triethylamine; In benzene;