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Merck
CN

263605

Sigma-Aldrich

1-丁基磺酰氯

98%

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About This Item

线性分子式:
CH3(CH2)3SO2Cl
CAS号:
分子量:
156.63
Beilstein:
1748742
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

蒸汽压

0.5 mmHg ( 20 °C)

质量水平

检测方案

98%

形式

liquid

折射率

n20/D 1.454 (lit.)

bp

80-81 °C/9 mmHg (lit.)

密度

1.208 g/mL at 25 °C (lit.)

SMILES字符串

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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应用

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

象形图

CorrosionExclamation mark

警示用语:

Danger

危险声明

危险分类

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

174.2 °F

闪点(°C)

79 °C

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

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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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