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Key Documents

P21404

Sigma-Aldrich

Phenyl carbamate

97%

Synonym(s):

O-Phenyl carbamate

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About This Item

Linear Formula:
H2NCO2C6H5
CAS Number:
Molecular Weight:
137.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

powder

mp

149-152 °C (lit.)

SMILES string

NC(=O)Oc1ccccc1

InChI

1S/C7H7NO2/c8-7(9)10-6-4-2-1-3-5-6/h1-5H,(H2,8,9)

InChI key

BSCCSDNZEIHXOK-UHFFFAOYSA-N

Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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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