• Product Name(S)-3,4-dihydro-6-chloro-4-hydroxy-2H-thieno[3,2-e]-1,2-thiazine-1,1-dioxide
  • CasNo. 160982-16-1
  • MFC6H6ClNO3S2
  • MW239.704
  • Purity
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Product Details

CasNo: 160982-16-1

MF: C6H6ClNO3S2

Reputable manufacturer supply (S)-3,4-dihydro-6-chloro-4-hydroxy-2H-thieno[3,2-e]-1,2-thiazine-1,1-dioxide 160982-16-1 in stock with high standard

  • Molecular Formula:C6H6ClNO3S2
  • Molecular Weight:239.704
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:128.0 to 132.0 °C 
  • Refractive Index:1.664 
  • Boiling Point:427.885 °C at 760 mmHg 
  • PKA:9.72±0.40(Predicted) 
  • Flash Point:212.578 °C 
  • PSA:103.02000 
  • Density:1.746 g/cm3 
  • LogP:2.13640 

(S)-6-CHLORO-1,1-DIOXO-1,2,3,4-TETRAHYDRO-1LAMBDA*6*-THIENO[3,2-E][1,2]THIAZIN-4-OL(Cas 160982-16-1) Usage

General Description

(S)-6-Chloro-1,1-dioxo-1,2,3,4-tetrahydro-1lambda*6*-thieno[3,2-e][1,2]thiazin-4-ol is a chemical compound with the molecular formula C4H3ClNO3S2. It is a heterocyclic compound that contains both oxygen and sulfur atoms in its ring structure. (S)-6-CHLORO-1,1-DIOXO-1,2,3,4-TETRAHYDRO-1LAMBDA*6*-THIENO[3,2-E][1,2]THIAZIN-4-OL may have potential pharmaceutical applications due to its unique structure, and it could be used in the development of new drugs or as a reagent in chemical reactions. Further research and analysis are necessary to fully understand the properties and potential uses of this chemical compound.

InChI:InChI=1/C6H6ClNO3S2/c7-5-1-3-4(9)2-8-13(10,11)6(3)12-5/h1,4,8-9H,2H2/t4-/m1/s1

160982-16-1 Relevant articles

Enantioselective synthesis of brinzolamide (AL-4862), a new topical carbonic anhydrase inhibitor. The "DCAT Route" to thiophenesulfonamides

Conrow, Raymond E.,Dean, W. Dennis,Zinke, Paul W.,Deason, Michael E.,Sproull, Steven J.,Dantanarayana, Anura P.,DuPriest, Mark T.

, p. 114 - 120 (2013/09/08)

A large scale synthesis of the topical c...

Sulfonamides useful as carbonic anhydrase inhibitors

-

, (2008/06/13)

Sulfonamides and pharmaceutical composit...

160982-16-1 Process route

3-(2-Bromoacetyl)-5-chloro-thiophene-2-sulfonamide
160982-11-6

3-(2-Bromoacetyl)-5-chloro-thiophene-2-sulfonamide

(S)-3,4-dihydro-6-chloro-4-hydroxy-4H-thieno[3,2-e]-1,2-thiazine-1,1-dioxide
160982-16-1,171274-01-4

(S)-3,4-dihydro-6-chloro-4-hydroxy-4H-thieno[3,2-e]-1,2-thiazine-1,1-dioxide

Conditions
Conditions Yield
3-(2-Bromoacetyl)-5-chloro-thiophene-2-sulfonamide; With B-chlorodiisopinocampheylborane; In tert-butyl methyl ether; at -40 - -32 ℃; for 3.5h; Inert atmosphere;
With sodium hydroxide; In tert-butyl methyl ether; water; at 0 - 22 ℃; for 2h; enantioselective reaction;
77%
3-(2-Bromoacetyl)-5-chloro-thiophene-2-sulfonamide
160982-11-6

3-(2-Bromoacetyl)-5-chloro-thiophene-2-sulfonamide

(+)-β-chlorodiisopino-campheylborane

(+)-β-chlorodiisopino-campheylborane

tert-butyl methyl ether
1634-04-4

tert-butyl methyl ether

carbon dioxide
124-38-9,18923-20-1

carbon dioxide

(S)-3,4-dihydro-6-chloro-4-hydroxy-4H-thieno[3,2-e]-1,2-thiazine-1,1-dioxide
160982-16-1,171274-01-4

(S)-3,4-dihydro-6-chloro-4-hydroxy-4H-thieno[3,2-e]-1,2-thiazine-1,1-dioxide

Conditions
Conditions Yield
With hydrogenchloride; sodium hydroxide; In toluene;

160982-16-1 Upstream products

  • 160982-11-6
    160982-11-6

    3-(2-Bromoacetyl)-5-chloro-thiophene-2-sulfonamide

  • 1634-04-4
    1634-04-4

    tert-butyl methyl ether

  • 124-38-9
    124-38-9

    carbon dioxide

  • 36157-40-1
    36157-40-1

    3-acetyl-2,5-dichlorothiophene

160982-16-1 Downstream products

  • 171273-35-1
    171273-35-1

    2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamine 1,1-dioxide

  • 138890-62-7
    138890-62-7

    brinzolamide

  • 154127-42-1
    154127-42-1

    (S)-3,4-dihydro-4-hydroxy-2(3-methoxypropyl)-4H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide

  • 160982-13-8
    160982-13-8

    (S)-3,4-dihydro-6-chloro-4-hydroxy-2-(3-methoxypropyl)-4H-thieno[3,2-e]-1,2-thiazine 1,1-dioxide

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