263605
1-Butanesulfonyl chloride
98%
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About This Item
Linear Formula:
CH3(CH2)3SO2Cl
CAS Number:
Molecular Weight:
156.63
EC Number:
219-204-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1748742
MDL number:
Assay:
98%
Form:
liquid
InChI key
WEDIIKBPDQQQJU-UHFFFAOYSA-N
InChI
1S/C4H9ClO2S/c1-2-3-4-8(5,6)7/h2-4H2,1H3
SMILES string
CCCCS(Cl)(=O)=O
vapor pressure
0.5 mmHg ( 20 °C)
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.)
Quality Level
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
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
174.2 °F - closed cup
flash_point_c
79 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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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