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Merck
CN

V001425

靛红

p.a.

别名:

NSC 9262, 吲哚-2,3-二酮, 靛红

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关于此项目

经验公式(希尔记法):
C8H5NO2
化学文摘社编号:
分子量:
147.13
EC Number:
202-077-8
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
383659
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InChI

1S/C8H5NO2/c10-7-5-3-1-2-4-6(5)9-8(7)11/h1-4H,(H,9,10,11)

InChI key

JXDYKVIHCLTXOP-UHFFFAOYSA-N

SMILES string

O=C1Nc2ccccc2C1=O

grade

p.a.

mp

193-195 °C (dec.) (lit.)

Quality Level

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存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

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S K Bhattacharya et al.
Indian journal of experimental biology, 36(12), 1195-1200 (1999-03-27)
Stress is often associated with water retention and its resolution with diuresis. The biological systems for the control of stress and water balance are very closely related. Corticotrophin releasing hormone (CRH) and arginine vasopressin (AVP) are co-localised in the hypothalamus
Isatin--a new biological factor.
V Glover et al.
Indian journal of experimental biology, 29(1), 1-5 (1991-01-01)
K L Vine et al.
Anti-cancer agents in medicinal chemistry, 9(4), 397-414 (2009-05-16)
Isatin (1H-indole-2,3-dione) and its derivatives demonstrate a diverse array of biological and pharmacological activities including anticonvulsant, antibacterial, antifungal, antiviral and anticancer properties. This broad spectrum of biochemical targets has been facilitated by the synthetic versatility of isatin, which has allowed
V Glover et al.
Voprosy meditsinskoi khimii, 43(6), 515-521 (1998-03-21)
Isatin is an endogenous compound recently discovered in mammalian tissues and body fluids. It has a distinct distribution in rat brain, with a highest concentration, in the hippocampus, of 0.1 microgram/g. Its origin and metabolic pathways remain unclear. In vitro
Shuichi Nakamura et al.
Organic letters, 17(1), 106-109 (2014-12-20)
The first catalytic enantioselective addition of thiols to ketimines derived from isatins has been developed. Excellent yields and enantioselectivities were observed for the reaction of various ketimines and thiols using a cinchona alkaloid sulfonamide catalyst. Both enantiomers of products could

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