Cas 486393-88-8,1H-Indole-3-carboxylic acid, 6-bromo-1-butyl-5-(cyanomethoxy)-2-[(methylphenylamino)methyl]-, ethyl ester

486393-88-8

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Basic information

Product Name: 1H-Indole-3-carboxylic acid, 6-bromo-1-butyl-5-(cyanomethoxy)-2-[(methylphenylamino)methyl]-, ethyl ester
Synonyms:
CAS NO:486393-88-8
Molecular Formula: C25H28BrN3O3
Molecular Weight: 498.42
EINECS: N/A
Product Categories: N/A
Mol File: 486393-88-8.mol

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: 1H-Indole-3-carboxylic acid, 6-bromo-1-butyl-5-(cyanomethoxy)-2-[(methylphenylamino)methyl]-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Indole-3-carboxylic acid, 6-bromo-1-butyl-5-(cyanomethoxy)-2-[(methylphenylamino)methyl]-, ethyl ester(486393-88-8)
EPA Substance Registry System: 1H-Indole-3-carboxylic acid, 6-bromo-1-butyl-5-(cyanomethoxy)-2-[(methylphenylamino)methyl]-, ethyl ester(486393-88-8)

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: 486393-88-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 486393-88-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,6,3,9 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 486393-88:
(8*4)+(7*8)+(6*6)+(5*3)+(4*9)+(3*3)+(2*8)+(1*8)=208
208 % 10 = 8
So 486393-88-8 is a valid CAS Registry Number.

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486393-88-8Relevant academic research and scientific papers

Synthesis and antimicrobial activity of new 6-bromo-1-butyl-3-ethoxycarbonyl-2-(N-methyl-N-phenylamino)methyl-5-(1,2,3,4- tetrazol-5-YL)methoxyindole

Gadaginamath,Patil

, p. 99 - 102 (2007/10/03)

6-Bromo-1-butyl-3-ethoxycarbonyl-2-methylindol-5-yloxyacetonitrile (2) was prepared by reacting 5-hydroxy-indole with chloroacetonitrile in refluxing acetone with K2CO3 and catalytic amount of KI. Compound 2 was then subjected to reg

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