추천 제품
Quality Level
분석
95%
불순물
<3% acetone
mp
175 °C (dec.) (lit.)
작용기
ketone
SMILES string
Oc1ccc2C(=O)CCc2c1
InChI
1S/C9H8O2/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5,10H,1,4H2
InChI key
ZRKQOVXGDIZYDS-UHFFFAOYSA-N
일반 설명
5-Hydroxy-1-indanone is a 1-indanone derivative.
애플리케이션
5-Hydroxy-1-indanone may be used in the preparation of (5-hydroxy-indan-(1E)-ylidene)-acetic acid and 5-[2-(phenyl)ethoxy]-1-indanone. It may be used as a starting material in the multi-step synthesis of 5H-indeno[1,2-c]pyridazin-5-one analogs.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
Geometric and solvent effects on intramolecular phenolic hydrogen abstraction by carbonyl n,p* and p,p* triplets.
Canadian Journal of Chemistry, 79(12), 1851-1863 (2001)
On the involvement of single-bond rotation in the primary photochemistry of photoactive yellow protein.
Biophysical Journal, 101(5), 1184-1192 (2011)
European journal of medicinal chemistry, 46(12), 6104-6111 (2011-10-25)
Previous studies on 5H-indeno[1,2-c]pyridazin-5-one derivatives as inhibitors of MAO-B revealed that it was possible to increase the MAO-B inhibitory potency of 5H-indeno[1,2-c]pyridazin-5-ones by substituting the central heterocycle in the 3-position or C-8 with lipophilic groups which occupy the substrate cavity
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