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736686

Sigma-Aldrich

Allyl carbamate

95%

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About This Item

Empirical Formula (Hill Notation):
C4H7NO2
CAS Number:
Molecular Weight:
101.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

95%

form

liquid

refractive index

n20/D 1.454

density

1.077 g/mL at 25 °C

storage temp.

−20°C

SMILES string

NC(=O)OCC=C

InChI

1S/C4H7NO2/c1-2-3-7-4(5)6/h2H,1,3H2,(H2,5,6)

InChI key

OCAAZRFBJBEVPS-UHFFFAOYSA-N

pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

212.0 °F

flash_point_c

100 °C


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M Cheng et al.
Cancer research, 42(6), 2165-2167 (1982-06-01)
In vivo sister chromatid exchange (SCE) induction by vinyl and allyl carbamates was examined in alveolar macrophage, bone marrow, and regenerating liver cells of C57BL/6J x DBA/2J F1 mice. Allyl carbamate was effective in producing increases in SCE frequencies (relative
Ruthenium-induced allylcarbamate cleavage in living cells.
Craig Streu et al.
Angewandte Chemie (International ed. in English), 45(34), 5645-5648 (2006-07-21)
Ming Yan et al.
Chemical reviews, 117(21), 13230-13319 (2017-10-11)
Electrochemistry represents one of the most intimate ways of interacting with molecules. This review discusses advances in synthetic organic electrochemistry since 2000. Enabling methods and synthetic applications are analyzed alongside innate advantages as well as future challenges of electroorganic chemistry.

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