Cas 1395347-27-9,1-(1-tert-butoxycarbonyl-5-chloro-1H-indol-3-yl)-6,7-dihydroxy-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester

1395347-27-9

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Basic information

Product Name: 1-(1-tert-butoxycarbonyl-5-chloro-1H-indol-3-yl)-6,7-dihydroxy-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester
Synonyms:
CAS NO:1395347-27-9
Molecular Formula:
Molecular Weight: 472.925
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: 1-(1-tert-butoxycarbonyl-5-chloro-1H-indol-3-yl)-6,7-dihydroxy-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-(1-tert-butoxycarbonyl-5-chloro-1H-indol-3-yl)-6,7-dihydroxy-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester(1395347-27-9)
EPA Substance Registry System: 1-(1-tert-butoxycarbonyl-5-chloro-1H-indol-3-yl)-6,7-dihydroxy-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester(1395347-27-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1395347-27-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1395347-27-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,5,3,4 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1395347-27:
(9*1)+(8*3)+(7*9)+(6*5)+(5*3)+(4*4)+(3*7)+(2*2)+(1*7)=189
189 % 10 = 9
So 1395347-27-9 is a valid CAS Registry Number.

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1395347-27-9Relevant academic research and scientific papers

Synthesis of C-1 indol-3-yl substituted tetrahydroisoquinoline derivatives via a Pictet-Spengler approach

Larsson, Rikard,Blanco, Narda,Johansson, Martin,Sterner, Olov

, p. 4966 - 4970 (2012)

A protocol for the diastereoselective synthesis of C-1 indol-3-yl substituted tetrahydroisoquinoline derivatives via Pictet-Spengler condensation with L-DOPA or l-DOPA derivatives and 1H-indole-3-carbaldehydes is presented. The protocol is used for the successful synthesis of several tetrahydroisoquinolines as well as diketopiperazine fused analogues.

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