Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  API >  Synthetic Anti-infective Drugs >  Sulfonamides and synergist >  1,4-BUTANESULTAM

1,4-BUTANESULTAM

Basic information Safety Supplier Related

1,4-BUTANESULTAM Basic information

Product Name:
1,4-BUTANESULTAM
Synonyms:
  • 2H-1,2-Thiazine,tetrahydro-, 1,1-dioxide
  • Thiazinane 1,1-dioxide
  • 1,2-thiazinane 1,1-dioxide
  • 1,1-Dioxotetrahydro-2H-1,2-thiazine, 1,4-Butanesultam
  • 1,1-DIOXO-TETRAHYDRO-2H-1,2-THIAZINE
  • 1,4-BUTANESULTAM
  • 1,4-BUTANESULTAM USP/EP/BP
  • 1lambda6,2-thiazinane-1,1-dione
CAS:
37441-50-2
MF:
C4H9NO2S
MW:
135.18
Product Categories:
  • blocks
  • BuildingBlocks
  • Sulfonamides
Mol File:
37441-50-2.mol
More
Less

1,4-BUTANESULTAM Chemical Properties

Melting point:
74-84°C
Boiling point:
143-145 °C(Press: 0.8 Torr)
Density 
1.239±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
11.70±0.20(Predicted)
color 
White to Light yellow
InChI
InChI=1S/C4H9NO2S/c6-8(7)4-2-1-3-5-8/h5H,1-4H2
InChIKey
DNGMYXZLJGHHOM-UHFFFAOYSA-N
SMILES
S1(=O)(=O)CCCCN1
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
Hazard Note 
Irritant
HS Code 
2941100000
More
Less

1,4-BUTANESULTAM Usage And Synthesis

Synthesis Reference(s)

The Journal of Organic Chemistry, 52, p. 2162, 1987 DOI: 10.1021/jo00387a008

Synthesis

3144-06-7

37441-50-2

At room temperature, 4-chloro-1-butanesulfonamide (D5) (31 g, 200 mmol, 1.0 eq.) was dissolved in ethanol (500 mL), followed by the addition of sodium ethoxide (14.9 g, 220 mmol, 1.1 eq.). The reaction mixture was heated to reflux for 5 h. After completion of the reaction it was cooled to room temperature and concentrated under reduced pressure. The residual solid was fully extracted by adding dichloromethane to the residual solid and concentrated under reduced pressure after combining the organic phases. The resulting solid was ground with ether to afford tetrahydro-2H-1,2-thiazine 1,1-dioxide (D6) (18.7 g, 69% yield) as a light brown solid, which was used directly in the subsequent reaction without further purification.

References

[1] Patent: WO2004/111022, 2004, A1. Location in patent: Page/Page column 15
[2] Journal of Organic Chemistry, 1987, vol. 52, # 11, p. 2162 - 2166

1,4-BUTANESULTAMSupplier

Accela ChemBio Co.,Ltd. Gold
Tel
021-50795510 4000665055
Email
syeu@accelachem.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com