Cas 58956-41-5,3-hydroxy-3-(2-methyl-1H-indol-3-yl)-1-methylindolin-2-one

58956-41-5

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Basic information

Product Name: 3-hydroxy-3-(2-methyl-1H-indol-3-yl)-1-methylindolin-2-one
Synonyms: 3-hydroxy-3-(2-methyl-1H-indol-3-yl)-1-methylindolin-2-one
CAS NO:58956-41-5
Molecular Formula:
Molecular Weight: 292.337
EINECS: N/A
Product Categories: N/A
Mol File: 58956-41-5.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-hydroxy-3-(2-methyl-1H-indol-3-yl)-1-methylindolin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-hydroxy-3-(2-methyl-1H-indol-3-yl)-1-methylindolin-2-one(58956-41-5)
EPA Substance Registry System: 3-hydroxy-3-(2-methyl-1H-indol-3-yl)-1-methylindolin-2-one(58956-41-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 58956-41-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 58956-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,5 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58956-41:
(7*5)+(6*8)+(5*9)+(4*5)+(3*6)+(2*4)+(1*1)=175
175 % 10 = 5
So 58956-41-5 is a valid CAS Registry Number.

58956-41-5Upstream product

95-20-5 2-methyl-1H-indole

58956-41-5Downstream Products

58956-41-5Relevant articles and documents

3-Hydroxy-3-((3-methyl-4-nitroisoxazol-5-yl)methyl)indolin-2-one as a versatile intermediate for retro-Henry and Friedel-Crafts alkylation reactions in aqueous medium

Nagaraju, Sakkani,Sathish, Kota,Paplal, Banoth,Satyanarayana, Neeli,Kashinath, Dhurke

, p. 14045 - 14050 (2019)

The first example of a retro-Henry type reaction is reported using 3-hydroxy-3-((3-methyl-4-nitroisoxazol-5-yl)methyl)indolin-2-ones which are prepared via catalyst-free Henry reaction of 3,5-dimethyl-4-nitroisoxazole and isatin. These compounds were used

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