추천 제품
grade
purum
분석
≥98.0% (GC)
refractive index
n20/D 1.457 (lit.)
n20/D 1.457
bp
143-145 °C (lit.)
density
1.324 g/mL at 20 °C
1.33 g/mL at 25 °C (lit.)
SMILES string
ClCCC(Cl)=O
InChI
1S/C3H4Cl2O/c4-2-1-3(5)6/h1-2H2
InChI key
INUNLMUAPJVRME-UHFFFAOYSA-N
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애플리케이션
3-Chloropropionyl chloride has been used in:
- microwave-promoted liquid-phase synthesis of 3,5-disubstituted 2-thioxotetrahydropyrimidin-4-ones
- preparation of hydrophilic and macroporous polymer resins modified with isothiocyanate groups
- synthesis of diethylaminopropionamido-hydroxy-anthraquinones, which are potential anticancer agents
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A
보충제 위험성
Storage Class Code
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
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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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