736686
Allyl carbamate
95%
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About This Item
Empirical Formula (Hill Notation):
C4H7NO2
CAS Number:
Molecular Weight:
101.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
218-309-6
MDL number:
InChI key
OCAAZRFBJBEVPS-UHFFFAOYSA-N
InChI
1S/C4H7NO2/c1-2-3-7-4(5)6/h2H,1,3H2,(H2,5,6)
SMILES string
NC(=O)OCC=C
assay
95%
form
liquid
refractive index
n20/D 1.454
density
1.077 g/mL at 25 °C
storage temp.
−20°C
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
212.0 °F
flash_point_c
100 °C
Regulatory Information
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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
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.
Ruthenium-induced allylcarbamate cleavage in living cells.
Craig Streu et al.
Angewandte Chemie (International ed. in English), 45(34), 5645-5648 (2006-07-21)
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