17631
3-Bromomethyl-7-methoxy-1,4-benzoxazin-2-one
BioReagent, suitable for fluorescence, ≥97.0%
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About This Item
Empirical Formula (Hill Notation):
C10H8BrNO3
CAS Number:
Molecular Weight:
270.08
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
product line
BioReagent
assay
≥97.0%
mp
144-148 °C
fluorescence
λex 343 nm; λem 430 nm
suitability
suitable for fluorescence
storage temp.
2-8°C
SMILES string
COc1ccc2N=C(CBr)C(=O)Oc2c1
InChI
1S/C10H8BrNO3/c1-14-6-2-3-7-9(4-6)15-10(13)8(5-11)12-7/h2-4H,5H2,1H3
InChI key
XFCZURAACWKKIH-UHFFFAOYSA-N
Other Notes
Highly sensitive fluorescent derivatizing agent for carboxylic acids; detection at 440 nm with excitation at 345 nm
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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J Yamada et al.
Analytical biochemistry, 199(1), 132-136 (1991-11-15)
A sensitive nonradioisotopic method is reported for measuring microsomal lauric acid omega-hydroxylation activity. The assay is based upon separation and detection of 12-hydroxylauric acid formed by means of high-performance liquid chromatography following fluorescence labeling of the carboxyl group with 3-bromomethyl-7-methoxy-1,4-benzoxazin-2-one
A. Nakanishi et al.
Journal of Chromatography A, 591, 159-159 (1992)
Kwan Soo Kim et al.
Journal of the American Chemical Society, 130(26), 8537-8547 (2008-06-06)
An efficient direct one-pot glycosylation method with anomeric hydroxy sugars as glycosyl donors employing phthalic anhydride and triflic anhydride as activating agents has been developed. Thus, highly stereoselective beta-mannopyranosylations were achieved by the reaction of 2,3-di-O-benzyl-4,6-O-benzylidene-D-mannopyranose (2) with phthalic anhydride
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