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630659

Sigma-Aldrich

Allyl phenyl carbonate

97%

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About This Item

Empirical Formula (Hill Notation):
C10H10O3
CAS Number:
16308-68-2
Molecular Weight:
178.18
MDL number:
MFCD07784342
UNSPSC Code:
12352100
PubChem Substance ID:
24882327
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.4990 (lit.)

bp

67-70 °C/0.3 mmHg (lit.)

density

1.096 g/mL at 25 °C (lit.)

SMILES string

C=CCOC(=O)Oc1ccccc1

InChI

1S/C10H10O3/c1-2-8-12-10(11)13-9-6-4-3-5-7-9/h2-7H,1,8H2

InChI key

ORUWSEKEVGOAQR-UHFFFAOYSA-N

General description

Allyl phenyl carbonate can be obtained via by reacting phenyl chloroformate and allyl alcohol in presence of pyridine.

Application

Allyl phenyl carbonate can react with (2-alkynyl)phenylisocyanate, catalyzed P(0)/Cu(I) system to give the corresponding indole.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H317,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

>230.0 °F

Flash Point(C)

> 110 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

630659-BULK:
630659-VAR:
630659-1G:
630659-5G:

Certificates of Analysis (COA)

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"A New Pd0?CuI Bimetallic Catalyst for the Synthesis of Indoles from Isocyanates and Allyl Carbonates"
Kamijo S and Yamamoto Y
Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 114(17), 3364-3367 (2002)
?Selective synthesis of carbamate protected polyamines using alkyl phenyl carbonates"
Pittelkow M, et al.
Synthesis, 2002(15), 2195- 2202 (2002)

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