Cas 1229291-51-3,methyl 3-((R)-((R)-5,5-dimethyltetrahydrofuran-2-yl)(2-hydroxyphenyl)methyl)-1-methyl-1H-indole-6-carboxylate

1229291-51-3

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Basic information

Product Name: methyl 3-((R)-((R)-5,5-dimethyltetrahydrofuran-2-yl)(2-hydroxyphenyl)methyl)-1-methyl-1H-indole-6-carboxylate
Synonyms: methyl 3-((R)-((R)-5,5-dimethyltetrahydrofuran-2-yl)(2-hydroxyphenyl)methyl)-1-methyl-1H-indole-6-carboxylate
CAS NO:1229291-51-3
Molecular Formula:
Molecular Weight: 393.483
EINECS: N/A
Product Categories: N/A
Mol File: 1229291-51-3.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: methyl 3-((R)-((R)-5,5-dimethyltetrahydrofuran-2-yl)(2-hydroxyphenyl)methyl)-1-methyl-1H-indole-6-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 3-((R)-((R)-5,5-dimethyltetrahydrofuran-2-yl)(2-hydroxyphenyl)methyl)-1-methyl-1H-indole-6-carboxylate(1229291-51-3)
EPA Substance Registry System: methyl 3-((R)-((R)-5,5-dimethyltetrahydrofuran-2-yl)(2-hydroxyphenyl)methyl)-1-methyl-1H-indole-6-carboxylate(1229291-51-3)

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: 1229291-51-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1229291-51-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,9,2,9 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1229291-51:
(9*1)+(8*2)+(7*2)+(6*9)+(5*2)+(4*9)+(3*1)+(2*5)+(1*1)=153
153 % 10 = 3
So 1229291-51-3 is a valid CAS Registry Number.

1229291-51-3Upstream product

1204-32-6 methyl 1-methylindole-6-carboxylate

1229291-51-3Downstream Products

1229291-51-3Relevant articles and documents

Synthesis and preliminary biological studies of 3-substituted indoles accessed by a palladium-catalyzed enantioselective alkene difunctionalization reaction

Pathak, Tejas P.,Gligorich, Keith M.,Welm, Bryan E.,Sigman, Matthew S.

supporting information; experimental part, p. 7870 - 7871 (2010/08/05)

A unique alkene difunctionalization reaction that allows rapid construction of molecular complexity around the biologically relevant indole framework has been developed. The reaction proceeds with up to 87% yield, 99:1 er, and >20:1 dr. Evaluation of several of the compounds revealed promising anticancer activity against MCF-7 cells.

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