H53704
N-Hydroxyphthalimide
97%, for peptide synthesis
동의어(들):
2-Hydroxy-1H-isoindole-1,3(2H)-dione, 2-Hydroxyisoindole-1,3-dione, 2-Hydroxyphthalimide
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모든 사진(4)
About This Item
실험식(Hill 표기법):
C8H5NO3
CAS Number:
Molecular Weight:
163.13
Beilstein:
131208
EC Number:
MDL number:
UNSPSC 코드:
12352005
PubChem Substance ID:
NACRES:
NA.22
추천 제품
제품명
N-Hydroxyphthalimide, 97%
Quality Level
분석
97%
양식
crystalline
반응 적합성
reaction type: Addition Reactions
mp
233 °C (dec.) (lit.)
응용 분야
peptide synthesis
SMILES string
ON1C(=O)c2ccccc2C1=O
InChI
1S/C8H5NO3/c10-7-5-3-1-2-4-6(5)8(11)9(7)12/h1-4,12H
InChI key
CFMZSMGAMPBRBE-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
For preparation of amine nucleosides for coupling into non-anionic, anti-sense oligonucleosides.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
Tetrahedron Letters, 33, 2645-2645 (1992)
Application of a dual linker with a reference cleavage site to discover a new reaction between amines and N-hydroxyphthalimide.
Viktor Krchnák et al.
Journal of combinatorial chemistry, 7(4), 523-525 (2005-07-12)
Guanyu Yang et al.
Journal of the American Chemical Society, 126(34), 10542-10543 (2004-08-26)
Hydrocarbon oxyfunctionalization is a crucial industrial process. Most metallic catalysts require higher temperatures and often show lower selectivities. One of the intellectual approaches is the mimicry for bio-oxidation. We have established a biomimetic system with a nonmetallic redox center, composed
Markus Tonigold et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(31), 8671-8695 (2011-06-21)
Crystal structures of two metal-organic frameworks (MFU-1 and MFU-2) are presented, both of which contain redox-active Co(II) centres coordinated by linear 1,4-bis[(3,5-dimethyl)pyrazol-4-yl] ligands. In contrast to many MOFs reported previously, these compounds show excellent stability against hydrolytic decomposition. Catalytic turnover
Riyuan Lin et al.
Organic letters, 14(16), 4158-4161 (2012-08-03)
A metal-free N-hydroxyphthalimide (NHPI) catalyzed aerobic oxidative cleavage of olefins has been developed. Molecular oxygen is used as the oxidant and reagent for this oxygenation reaction. This methodology has prevented the use of toxic metals or overstoichiometric amounts of traditional
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