669393
N-Methyl-O-benzoylhydroxylamine hydrochloride
97%
Synonym(s):
Benzoic acid N-hydroxymethylamine ester hydrochloride
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
(C6H5)CO2(NHCH3) HCl
CAS Number:
Molecular Weight:
187.62
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22
Assay:
97%
Form:
solid
SMILES string
[Cl-].C[NH2+]OC(=O)c1ccccc1
InChI
1S/C8H9NO2.ClH/c1-9-11-8(10)7-5-3-2-4-6-7;/h2-6,9H,1H3;1H
InChI key
FTCDQNQIGUCFSA-UHFFFAOYSA-N
assay
97%
form
solid
mp
133 °C (dec.)
functional group
amine, phenyl
storage temp.
2-8°C
Application
Benzoylation Reagents Simple Tools for a-Oxygenation of Aldehydes and Ketones
Reactant for preparation of:
Reactant for preparation of:
- NHC-catalyzed redox esterification and cycloaddition reactions
- Pd/pyrrolidine-catalyzed Tsuji-Trost cyclization of aldehydes
- α-acyloxy ketones via oxyacylation reaction
Reagent for α-acyloxylation of aldehydes and ketones. The reagent is not sensitive to air and moisture.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Cory S Beshara et al.
Organic letters, 7(25), 5729-5732 (2005-12-03)
[chemical reaction: see text]. A simple, one-pot method for the alpha-acyloxylation of carbonyl compounds that proceeds at room temperature in the presence of both moisture and air has been developed. Treatment of a variety of aldehydes and both cyclic and
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service