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Merck
CN

26210

3-氯丙酰氯

purum, ≥98.0% (GC)

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线性分子式:
ClCH2CH2COCl
化学文摘社编号:
625-36-5
分子量:
126.97
EC Number:
210-890-4
UNSPSC Code:
12352100
PubChem Substance ID:
329752857
Beilstein/REAXYS Number:
635814
MDL number:
MFCD00000747
Assay:
≥98.0% (GC)

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InChI key

INUNLMUAPJVRME-UHFFFAOYSA-N

InChI

1S/C3H4Cl2O/c4-2-1-3(5)6/h1-2H2

SMILES string

ClCCC(Cl)=O

grade

purum

assay

≥98.0% (GC)

bp

143-145 °C (lit.)

density

1.324 g/mL at 20 °C, 1.33 g/mL at 25 °C (lit.)

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Application

3-氯丙酰氯已用于：
  • 微波促进的3,5-二取代2-硫代四氢嘧啶-4-酮的液相合成
  • 制备异硫氰酸酯基改性的亲水性和大孔聚合物树脂
  • 合成潜在抗癌药二乙氨基丙酰胺基-羟基蒽醌

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A

supp_hazards

EUH014

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 1

flash_point_f

158.9 °F - closed cup

flash_point_c

70.5 °C - closed cup

ppe

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

法规信息

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分析证书(COA)

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Wen-Ben Yeh et al.
Molecular diversity, 7(2-4), 185-198 (2004-02-12)
An efficient, microwave-assisted method for the liquid-phase combinatorial synthesis of 3,5-disubstituted thiohydantoins and 3,5-disubstituted 2-thioxotetrahydropyrimidin-4-ones has been developed. In synthesizing thiohydantoins, Fmoc-protected amino acids were coupled with polymer support and then deprotected to give primary amines. While in synthesizing thioxotetrahydropyrimidinones
M Hasegawa et al.
Biotechnology and bioengineering, 36(3), 219-223 (1990-07-01)
Hydrophilic and macroporous polymer resins composed of glycerylmethacrylate, styrene, and divinylbenzene were quite easily modified with isothiocyanate groups using a Friedel-Crafts reaction with 3-chloropropionyl chloride and subsequent nucleophilic reaction with KSCN. Alkaline phosphatase and trypsin could be covalently bound to
C Antonello et al.
Archiv der Pharmazie, 322(9), 541-544 (1989-09-01)
A number of new 9,10-anthracenediones were obtained, bearing one or two hydroxyl groups and one positively charged side chain at different positions of the aromatic ring system (compounds 1-5 in Chart 1). These derivatives resemble the anticancer agents mitoxantrone and

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