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About This Item
Linear Formula:
(CH3)2CHOCOCl
CAS Number:
Molecular Weight:
122.55
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
506416
Form:
liquid
form
liquid
Quality Level
concentration
1.0 M in toluene
density
0.892 g/mL at 25 °C
functional group
chloro
storage temp.
2-8°C
SMILES string
CC(C)OC(Cl)=O
InChI
1S/C4H7ClO2/c1-3(2)7-4(5)6/h3H,1-2H3
InChI key
IVRIRQXJSNCSPQ-UHFFFAOYSA-N
General description
Specific rates of solvolysis of isopropyl chloroformate in various solvents at 25°C has been reported.
Application
Isopropyl chloroform was used in the preparation of isopropyl cyclohexane via alkylation of cyclohexene. It was also used in the preparation of 10-isopropyloctadecanoic acid via reaction with oleic acid in the presence of ethylaluminum sesquichloride
signalword
Danger
Hazard Classifications
Acute Tox. 1 Inhalation - Aquatic Chronic 3 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Repr. 2 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 2 - STOT SE 3
target_organs
Central nervous system
Storage Class
3 - Flammable liquids
flash_point_f
42.8 °F - closed cup
flash_point_c
6 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
wgk
WGK 2
Regulatory Information
危险化学品
易制毒化学品(3类)
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Biermann et al.
Angewandte Chemie (International ed. in English), 38(24), 3675-3677 (2000-01-29)
The formal addition of propane to nonactivated double bonds can be achieved with isopropyl chloroformate (2) in the presence of Et(3)Al(2)Cl(3). Thus, a 1:1 mixture of 10-isopropyloctadecanoic acid (3) and the 9-regioisomer is formed from oleic acid (1). The reaction
Malcolm J D'Souza et al.
International journal of molecular sciences, 10(3), 862-879 (2009-04-29)
Specific rates of solvolysis at 25 degrees C for isopropyl chloroformate (1) in 24 solvents of widely varying nucleophilicity and ionizing power, plus literature values for studies in water and formic acid, are reported. Previously published solvolytic rate constants at
Hatem Salama Mohamed Ali et al.
Amino acids, 46(9), 2241-2257 (2014-06-19)
Whereas an abundance of literature is available on the occurrence of common proteinogenic amino acids (AAs) in edible fruits of the date palm (Phoenix dactylifera L.), recent reports on non-proteinogenic (non-coded) AAs and amino components are scarce. With emphasis on
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 335908-100ML | 04061836691967 |
| 335908-800ML | 04061836691974 |



