V900671
N-Hydroxyphthalimide
Vetec™, reagent grade, 97%
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About This Item
Empirical Formula (Hill Notation):
C8H5NO3
CAS Number:
Molecular Weight:
163.13
EC Number:
208-358-1
UNSPSC Code:
12352005
PubChem Substance ID:
Beilstein/REAXYS Number:
131208
MDL number:
InChI key
CFMZSMGAMPBRBE-UHFFFAOYSA-N
InChI
1S/C8H5NO3/c10-7-5-3-1-2-4-6(5)8(11)9(7)12/h1-4,12H
SMILES string
ON1C(=O)c2ccccc2C1=O
grade
reagent grade
product line
Vetec™
assay
97%
reaction suitability
reaction type: Addition Reactions
mp
233 °C (dec.) (lit.)
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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[Hydroxyphthalimide induced medicamentosa-like dermatitis in five patients].
Jian-fang Zou et al.
Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases, 24(10), 625-625 (2006-11-14)
James M Takacs et al.
Organic letters, 5(20), 3595-3598 (2003-09-26)
[reaction: see text] Screening combinations of five catalyst precursors with 13 phosphorus ligands identified cyclization catalysts that favor carbocyclization-trapping with N-hydroxyphthalimide over a competing cycloisomerization mode.
M H Lang et al.
Dermatosen in Beruf und Umwelt. Occupation and environment, 35(6), 212-213 (1987-11-01)
We report a case of a female laboratory worker in the chemical industry who acquired contact allergy to dicyclohexylcarbodiimide and N-hydroxyphthalimide. Both substances are used in the chemical synthesis of peptides. So far there have only been a few reports
V Krishnakumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(1), 110-115 (2008-01-26)
Single crystals of N-hydroxyphthalimide (NHPH) were obtained from saturated aqueous solutions of methanol and acetonitrile by slow cooling method. The grown crystals were bright and transparent. From the crystal structure analysis it can be inferred that the crystal belongs to
H M Petrassi et al.
Organic letters, 3(1), 139-142 (2001-06-30)
[figure: see text] A novel route to aryloxyamines via the copper-mediated cross-coupling of N-hydroxyphthalimide and phenylboronic acids is reported. The reaction is mediated by selected copper(I) and (II) salts in the presence of pyridine and is tolerant of several functional
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