Cas 500548-63-0,(R)-5-Bromo-2-(2-methoxy-acetyl)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester

500548-63-0

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Basic information

Product Name: (R)-5-Bromo-2-(2-methoxy-acetyl)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester
Synonyms: (R)-5-Bromo-2-(2-methoxy-acetyl)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester
CAS NO:500548-63-0
Molecular Formula:
Molecular Weight: 370.243
EINECS: N/A
Product Categories: N/A

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: (R)-5-Bromo-2-(2-methoxy-acetyl)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-5-Bromo-2-(2-methoxy-acetyl)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester(500548-63-0)
EPA Substance Registry System: (R)-5-Bromo-2-(2-methoxy-acetyl)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester(500548-63-0)

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: 500548-63-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 500548-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,5,4 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 500548-63:
(8*5)+(7*0)+(6*0)+(5*5)+(4*4)+(3*8)+(2*6)+(1*3)=120
120 % 10 = 0
So 500548-63-0 is a valid CAS Registry Number.

500548-63-0Upstream product

98167-06-7 (R)-(-)-2,3-Dihydro-1H-Indole-2-Carboxylic Acid

500548-63-0Downstream Products

500548-63-0Relevant academic research and scientific papers

Total synthesis of (+)-benzastatin E via diastereoselective Grignard addition to 2-acylindoline.

Toda, Narihiro,Ori, Mayuko,Takami, Kazuko,Tago, Keiko,Kogen, Hiroshi

, p. 269 - 271 (2003)

[reaction: see text] A stereoselective total synthesis of (+)-benzastatin E (1) is described. The synthesis involves a diastereoselective Grignard addition to 2-acylindoline 2, which is derived from commercially available (S)-2-indolinecarboxylic acid (3). The unknown absolute configuration of (+)-1 is determined as (9S,10R).

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