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About This Item
Linear Formula:
CH3(CH2)3SO2Cl
CAS Number:
Molecular Weight:
156.63
Beilstein:
1748742
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
vapor pressure
0.5 mmHg ( 20 °C)
Quality Level
Assay
98%
form
liquid
refractive index
n20/D 1.454 (lit.)
bp
80-81 °C/9 mmHg (lit.)
density
1.208 g/mL at 25 °C (lit.)
SMILES string
CCCCS(Cl)(=O)=O
InChI
1S/C4H9ClO2S/c1-2-3-4-8(5,6)7/h2-4H2,1H3
InChI key
WEDIIKBPDQQQJU-UHFFFAOYSA-N
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Application
1-Butanesulfonyl chloride has been used in the preparation of:
- ethyl 2-(1-butanesulfonamido)pent-4-yn-l-oate
- 1-butanesulfonamid-N,N′-1,2-ethanediylbis
- 1-butanesulfonamide-N,N′-1,3-propanediylbis
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
174.2 °F - closed cup
Flash Point(C)
79 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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N J Liverton et al.
Bioorganic & medicinal chemistry letters, 8(5), 483-486 (1999-01-01)
The synthesis and biological activity of a series of 3,6-substituted quinazolinediones and quinazolinones are described. The potent activity of these compounds as platelet aggregation inhibitors demonstrates the utility of these structures as central templates for nonpeptide RGD mimics.
Neslihan Ozbek et al.
Bioorganic & medicinal chemistry, 15(15), 5105-5109 (2007-06-05)
A series of novel aliphatic sulfonamide derivatives (1-7) were synthesized and characterized by elemental analyses, FT-IR, (1)H NMR, (13)C NMR and LC-MS techniques. All the synthesized compounds were evaluated in vitro as antimicrobial agents against representative strains of Gram-positive (Staphylococcus
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