Cas 128593-40-8,6-bromo-5-methoxy-1H-indole-2-carboxylic acid ethyl ester

128593-40-8

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Basic information

Product Name: 6-bromo-5-methoxy-1H-indole-2-carboxylic acid ethyl ester
Synonyms: 6-bromo-5-methoxy-1H-indole-2-carboxylic acid ethyl ester
CAS NO:128593-40-8
Molecular Formula:
Molecular Weight: 298.136
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: 179-180 °C(Solv: ethyl ether (60-29-7))
Boiling Point: 424.2±40.0 °C(Predicted)
Flash Point: N/A
Appearance: N/A
Density: 1.517±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 6-bromo-5-methoxy-1H-indole-2-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-bromo-5-methoxy-1H-indole-2-carboxylic acid ethyl ester(128593-40-8)
EPA Substance Registry System: 6-bromo-5-methoxy-1H-indole-2-carboxylic acid ethyl ester(128593-40-8)

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: 128593-40-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128593-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,5,9 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 128593-40:
(8*1)+(7*2)+(6*8)+(5*5)+(4*9)+(3*3)+(2*4)+(1*0)=148
148 % 10 = 8
So 128593-40-8 is a valid CAS Registry Number.

128593-40-8Upstream product

128593-38-4 2-[(3-Bromo-4-methoxy-phenyl)-hydrazono]-propionic acid ethyl ester

128593-40-8Downstream Products

128593-40-8Relevant academic research and scientific papers

Palladium-Catalyzed Regioselective Hydrodebromination of Dibromoindoles: Application to the Enantioselective Synthesis of Indolodioxane U86192A

Chae, Junghyun,Buchwald, Stephen L.

, p. 3336 - 3339 (2007/10/03)

A novel approach to the selective preparation of 4-bromoindoles was developed via Pd(OAc)2/rac-BINAP catalytic reactions. A variety of 4,6-dibromoindoles were transformed to 4-bromoindoles with high regioselectivity. This methodology, along wit

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