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Merck
CN

433098

Sigma-Aldrich

5-溴-1-茚满酮

97%

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About This Item

经验公式(希尔记法):
C9H7BrO
CAS号:
分子量:
211.06
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

mp

126-129 °C (lit.)

官能团

bromo
ketone

SMILES字符串

Brc1ccc2C(=O)CCc2c1

InChI

1S/C9H7BrO/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5H,1,4H2

InChI key

KSONICAHAPRCMV-UHFFFAOYSA-N

一般描述

5-Bromo-1-indanone is a 1-indanone derivative. Its physical properties like density, freezing point and refractive index have been determined. It participates in the synthesis of the imidazolyl and triazolyl substituted biphenyl compounds.

象形图

Exclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

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Turn-On Fluorogenic Probes for the Selective and Quantitative Detection of the Cyanide Anion from Natural Sources.
Gomez T, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 8(6), 1271-1278 (2013)
Andrew K Takle et al.
Bioorganic & medicinal chemistry letters, 16(2), 378-381 (2005-11-02)
A novel triarylimidazole derivative, SB-590885 (33), bearing a 2,3-dihydro-1H-inden-1-one oxime substituent has been identified as a potent and extremely selective inhibitor of B-Raf kinase.
Y Zhuang et al.
Bioorganic & medicinal chemistry, 8(6), 1245-1252 (2000-07-15)
The synthesis of a new series of P450 17 inhibitors is described. The imidazol-1-yl compounds 5 showed strong inhibition of P450 17 rat and especially human enzyme, the most active compounds being 5ax, 5ay and 5bx with IC50 values of
Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 229-229 (2015)
Agustin Casimiro-Garcia et al.
Journal of medicinal chemistry, 54(12), 4219-4233 (2011-05-12)
Mining of an in-house collection of angiotensin II type 1 receptor antagonists to identify compounds with activity at the peroxisome proliferator-activated receptor-γ (PPARγ) revealed a new series of imidazo[4,5-b]pyridines 2 possessing activity at these two receptors. Early availability of the

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