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Key Documents

335908

Sigma-Aldrich

Isopropyl chloroformate solution

1.0 M in toluene

Sinonimo/i:

1-Methylethyl chloroformate, 2-Propyl chloroformate, Chloroformic acid isopropyl ester, Isopropoxycarbonyl chloride, Isopropyl carbonochloridate, Isopropyl chlorcarbonate, Isopropyl chlorocarbonate

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About This Item

Formula condensata:
(CH3)2CHOCOCl
Numero CAS:
Peso molecolare:
122.55
Beilstein:
506416
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Forma fisica

liquid

Concentrazione

1.0 M in toluene

Densità

0.892 g/mL at 25 °C

Temperatura di conservazione

2-8°C

Stringa SMILE

CC(C)OC(Cl)=O

InChI

1S/C4H7ClO2/c1-3(2)7-4(5)6/h3H,1-2H3
IVRIRQXJSNCSPQ-UHFFFAOYSA-N

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Descrizione generale

Specific rates of solvolysis of isopropyl chloroformate in various solvents at 25°C has been reported.

Applicazioni

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

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Central nervous system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

42.8 °F - closed cup

Punto d’infiammabilità (°C)

6 °C - closed cup

Dispositivi di protezione individuale

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


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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
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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
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