Cas 238750-16-8,1-(2-bromo-4,5-dimethoxy-benzyl)-1<i>H</i>-indole-2-carboxylic acid methyl ester

238750-16-8

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Basic information

Product Name: 1-(2-bromo-4,5-dimethoxy-benzyl)-1H-indole-2-carboxylic acid methyl ester
Synonyms: 1-(2-bromo-4,5-dimethoxy-benzyl)-1H-indole-2-carboxylic acid methyl ester
CAS NO:238750-16-8
Molecular Formula:
Molecular Weight: 404.26
EINECS: N/A
Product Categories: N/A
Mol File: 238750-16-8.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: 1-(2-bromo-4,5-dimethoxy-benzyl)-1H-indole-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-bromo-4,5-dimethoxy-benzyl)-1H-indole-2-carboxylic acid methyl ester(238750-16-8)
EPA Substance Registry System: 1-(2-bromo-4,5-dimethoxy-benzyl)-1H-indole-2-carboxylic acid methyl ester(238750-16-8)

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: 238750-16-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 238750-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,8,7,5 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 238750-16:
(8*2)+(7*3)+(6*8)+(5*7)+(4*5)+(3*0)+(2*1)+(1*6)=148
148 % 10 = 8
So 238750-16-8 is a valid CAS Registry Number.

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238750-16-8Relevant articles and documents

Intramolecular palladium-catalyzed cyclization of methyl 1-(2- bromobenzyl)indole-2-carboxylates: Synthesis of pratosine and hippadine

Miki, Yasuyoshi,Shirokoshi, Hideaki,Matsushita, Ko-ichi

, p. 4347 - 4348 (1999)

Palladium-catalyzed cyclization of methyl 1-(2-bromo-4,5-dimethoxy- benzyl)indole-2-carboxylate in the presence of potassium acetate in hot 1,4- dioxane gave a 7H-pyrrolo[3,2,1-de]phenanthridine derivative, which was converted to pratosine in four steps.

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