Home Cart Sign in  
Chemical Structure| 3306-62-5 Chemical Structure| 3306-62-5
Chemical Structure| 3306-62-5

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

2-Aminobenzenesulfonamide is a potent inhibitor of carbonic anhydrase B.

Synonyms: Orthanilamide; O-Sulfanilamide; Benzenesulfonamide

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of 2-Aminobenzenesulfonamide

CAS No. :3306-62-5
Formula : C6H8N2O2S
M.W : 172.21
SMILES Code : O=S(C1=CC=CC=C1N)(N)=O
Synonyms :
Orthanilamide; O-Sulfanilamide; Benzenesulfonamide
MDL No. :MFCD00007932
InChI Key :YAZSBRQTAHVVGE-UHFFFAOYSA-N
Pubchem ID :72894

Safety of 2-Aminobenzenesulfonamide

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of 2-Aminobenzenesulfonamide

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 3306-62-5 ]

[ 3306-62-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 89-20-3 ]
  • [ 3306-62-5 ]
  • [ 4512-17-8 ]
  • 2
  • [ 351003-48-0 ]
  • [ 3306-62-5 ]
  • [ 1161943-96-9 ]
YieldReaction ConditionsOperation in experiment
19% With pyridine; for 12.0h; 2-Aminobenzenesulfonamide (54 mg, 0.31 mmol) and <strong>[351003-48-0]3-chloro-2-fluoro-benzenesulfonyl chloride</strong> (47 mg, 0.21 mmol) were dissolved in pyridine (1 ml) and the reaction mixture was stirred for 12 h. The solvent was removed in vacuo and the residue was purified by HPLC to give the product (15 mg, 19%).1H NMR (400 MHz, DMSO-d6) delta ppm 9.72 (br. s., 1H), 7.90 (t, 1H), 7.78-7.86 (m, 2H), 7.73 (br. s., 2H), 7.51-7.58 (m, 1H), 7.46-7.51 (m, 1H), 7.39 (t, 1H), 7.26-7.34 (m, 1H);MS m/z M-H 363.
  • 3
  • [ 16375-88-5 ]
  • [ 3306-62-5 ]
  • N-(4-(1,1-dioxido-2H-benzo[e][1,2,4]thiadiazin-3-yl)phenyl)acetamide [ No CAS ]
  • 4
  • [ 3306-62-5 ]
  • [ 87220-68-6 ]
  • C25H17N3O2S [ No CAS ]
 

Historical Records

Categories