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433-17-0,MFCD11870742
Catalog No.:AA00DIA4

433-17-0 | Benzo[d]thiazole-2-sulfonamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
50mg
95%
3 weeks  
$259.00   $182.00
- +
100mg
95%
3 weeks  
$359.00   $252.00
- +
250mg
95%
3 weeks  
$486.00   $340.00
- +
500mg
95%
3 weeks  
$734.00   $514.00
- +
1g
95%
3 weeks  
$925.00   $648.00
- +
2.5g
95%
3 weeks  
$1,759.00   $1,232.00
- +
5g
95%
3 weeks  
$2,572.00   $1,800.00
- +
10g
95%
3 weeks  
$3,788.00   $2,652.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00DIA4
Chemical Name:
Benzo[d]thiazole-2-sulfonamide
CAS Number:
433-17-0
Molecular Formula:
C7H6N2O2S2
Molecular Weight:
214.2647
MDL Number:
MFCD11870742
SMILES:
NS(=O)(=O)c1nc2c(s1)cccc2
Properties
Computed Properties
 
Complexity:
285  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.3  

Downstream Synthesis Route

[1]Patent:US4416890,1983,A

Literature

Title: Synthesis, Characterization, and Biological Evaluation of certain 6-methyl-2(3H)-benzo-1, 3-thiazolyl-1'-ethylidene-2-(o, p- Substituted Acetophenones) Hydrazine Analogs.

Journal: Journal of young pharmacists : JYP 20100101

Title: Evaluation of antiproliferative activities and apoptosis induction caused by copper(II)-benzothiazolesulfonamide complexes in Jurkat T lymphocytes and Caco-2 cells.

Journal: Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry 20081101

Title: Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isozyme VII with aromatic and heterocyclic sulfonamides.

Journal: Bioorganic & medicinal chemistry letters 20050215

Title: Discovery of novel benzothiazolesulfonamides as potent inhibitors of HIV-1 protease.

Journal: Bioorganic & medicinal chemistry 20031103

Title: DNA cleavage studies of mononuclear and dinuclear copper(II) complexes with benzothiazolesulfonamide ligands.

Journal: Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry 20030701

Title: Carbonic anhydrase inhibitors. Preparation of potent sulfonamides inhibitors incorporating bile acid tails.

Journal: Bioorganic & medicinal chemistry letters 20020617

Quotation Request
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SDS
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Tags:433-17-0 Molecular Formula|433-17-0 MDL|433-17-0 SMILES|433-17-0 Benzo[d]thiazole-2-sulfonamide
Catalog No.: AA00DIA4
433-17-0,MFCD11870742
433-17-0 | Benzo[d]thiazole-2-sulfonamide
Pack Size： 50mg
Purity： 95%
3 weeks
$259.00 $182.00
Pack Size： 100mg
Purity： 95%
3 weeks
$359.00 $252.00
Pack Size： 250mg
Purity： 95%
3 weeks
$486.00 $340.00
Pack Size： 500mg
Purity： 95%
3 weeks
$734.00 $514.00
Pack Size： 1g
Purity： 95%
3 weeks
$925.00 $648.00
Pack Size： 2.5g
Purity： 95%
3 weeks
$1,759.00 $1,232.00
Pack Size： 5g
Purity： 95%
3 weeks
$2,572.00 $1,800.00
Pack Size： 10g
Purity： 95%
3 weeks
$3,788.00 $2,652.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00DIA4
Chemical Name: Benzo[d]thiazole-2-sulfonamide
CAS Number: 433-17-0
Molecular Formula: C7H6N2O2S2
Molecular Weight: 214.2647
MDL Number: MFCD11870742
SMILES: NS(=O)(=O)c1nc2c(s1)cccc2
Properties
Complexity: 285  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.3  
Downstream Synthesis Route
433-17-0    6108-17-4    86394-99-2 

[1]Patent:US4416890,1983,A

Literature fold

Title: Synthesis, Characterization, and Biological Evaluation of certain 6-methyl-2(3H)-benzo-1, 3-thiazolyl-1'-ethylidene-2-(o, p- Substituted Acetophenones) Hydrazine Analogs.

Journal: Journal of young pharmacists : JYP20100101

Title: Evaluation of antiproliferative activities and apoptosis induction caused by copper(II)-benzothiazolesulfonamide complexes in Jurkat T lymphocytes and Caco-2 cells.

Journal: Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry20081101

Title: Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isozyme VII with aromatic and heterocyclic sulfonamides.

Journal: Bioorganic & medicinal chemistry letters20050215

Title: Discovery of novel benzothiazolesulfonamides as potent inhibitors of HIV-1 protease.

Journal: Bioorganic & medicinal chemistry20031103

Title: DNA cleavage studies of mononuclear and dinuclear copper(II) complexes with benzothiazolesulfonamide ligands.

Journal: Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry20030701

Title: Carbonic anhydrase inhibitors. Preparation of potent sulfonamides inhibitors incorporating bile acid tails.

Journal: Bioorganic & medicinal chemistry letters20020617

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