P21404
Phenyl carbamate
97%
Synonym(s):
O-Phenyl carbamate
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About This Item
Linear Formula:
H2NCO2C6H5
CAS Number:
Molecular Weight:
137.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-737-1
MDL number:
Product Name
Phenyl carbamate, 97%
InChI key
BSCCSDNZEIHXOK-UHFFFAOYSA-N
InChI
1S/C7H7NO2/c8-7(9)10-6-4-2-1-3-5-6/h1-5H,(H2,8,9)
SMILES string
NC(=O)Oc1ccccc1
assay
97%
form
powder
mp
149-152 °C (lit.)
Quality Level
Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Amani Atayat et al.
Journal of separation science, 42(18), 3023-3032 (2019-06-30)
The aim of this work was to develop an efficient method for the selective extraction and analysis of fenoxycarb, a carbamate pesticide, in mussel samples using a molecularly imprinted solid-phase extraction device. The optimization of molecularly imprinted polymer synthesis was
Chin Fen Teo et al.
Glycobiology, 26(11), 1198-1208 (2016-04-14)
Previous studies utilizing PUGNAc, the most widely used β-N-acetylglucosaminidase (OGA) inhibitor to increase global O-N-acetylglucosamine (GlcNAc) levels, have reported a variety of effects including insulin resistance as a direct result of elevated O-GlcNAc levels. The notion of OGA inhibition causing
S A Adediran et al.
Archives of biochemistry and biophysics, 618, 23-31 (2017-01-29)
The best-studied amidase signature (AS) enzyme is probably fatty acid amide hydrolase (FAAH). Closely related to FAAH is mandelamide hydrolase (MAH), whose substrate specificity and mechanism of catalysis are described in this paper. First, we developed a convenient chromogenic substrate
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