246352
Methyl carbamate
98%
Sinónimos:
Urethylane
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About This Item
Productos recomendados
Quality Level
assay
98%
form
crystals
bp
176-177 °C (lit.)
mp
56-58 °C (lit.)
solubility
alcohol: freely soluble(lit.)
water: freely soluble(lit.)
functional group
amine
SMILES string
COC(N)=O
InChI
1S/C2H5NO2/c1-5-2(3)4/h1H3,(H2,3,4)
InChI key
GTCAXTIRRLKXRU-UHFFFAOYSA-N
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Application
Methyl carbamate was used in the synthesis of protected aminocyclopropanes.
signalword
Warning
hcodes
Hazard Classifications
Carc. 2 - Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Angewandte Chemie (International ed. in English), 52(38), 10060-10063 (2013-08-06)
Easy as 1,2,3: Reaction of methyl carbamate, triethyl orthoformate, and readily available alkenes provides a highly practical preparation of protected aminocyclopropanes. The reaction proceeds with preferential cis addition to alkenes, and cleavage of the methyl carbamate gives the free aminocyclopropanes
Genotoxicity data supporting the proposed metabolic activation of ethyl carbamate (urethane) to a carcinogen: the problem now posed by methyl carbamate.
Mutation research, 260(4), 307-308 (1991-08-01)
Methyl carbamate: negative results in mouse bone-marrow micronucleus test.
Mutation research, 260(4), 311-311 (1991-08-01)
Archives of environmental health, 50(6), 440-444 (1995-11-01)
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Ammonium perfluorooctanoate (APFOA) was investigated as an MS-friendly surfactant for the analysis of a mixture of ten N-methylcarbamates with MEKC-ESI-MS. Because of the relatively low boiling point of perfluorooctanoic acid ( approximately 190 degrees C), APFOA can be introduced into
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