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Merck
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文件

511544

Sigma-Aldrich

5-羟基-1-茚酮

95%

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About This Item

经验公式（希尔记法）:
C9H8O2
CAS号:
3470-49-3
分子量:
148.16
MDL號碼:
MFCD00857527
分類程式碼代碼:
12352100
PubChem物質ID:
24873548
NACRES:
NA.22

化驗

95%

雜質

<3% acetone

mp

175 °C (dec.) (lit.)

SMILES 字串

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 密鑰

ZRKQOVXGDIZYDS-UHFFFAOYSA-N

相关类别

一般說明

5-Hydroxy-1-indanone is a 1-indanone derivative.

應用

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.

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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Geometric and solvent effects on intramolecular phenolic hydrogen abstraction by carbonyl n,p* and p,p* triplets.
Lathioor EC and Leigh WJ.
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On the involvement of single-bond rotation in the primary photochemistry of photoactive yellow protein.
Stahl AD, et al.
Biophysical Journal, 101(5), 1184-1192 (2011)
J Reniers et al.
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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