V001425
Isatin
p.a.
Synonym(s):
2,3-Indolinedione, Isatine, NSC 9262
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About This Item
Empirical Formula (Hill Notation):
C8H5NO2
CAS Number:
Molecular Weight:
147.13
EC Number:
202-077-8
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
383659
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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Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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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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