Cas 1208321-05-4,tert-butyl 1,4-dimethyl-2-((2-methyl-1H-indol-3-yl)(phenyl)methyl)-3,6-dioxopiperazine-2-carboxylate

1208321-05-4

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Basic information

Product Name: tert-butyl 1,4-dimethyl-2-((2-methyl-1H-indol-3-yl)(phenyl)methyl)-3,6-dioxopiperazine-2-carboxylate
Synonyms: tert-butyl 1,4-dimethyl-2-((2-methyl-1H-indol-3-yl)(phenyl)methyl)-3,6-dioxopiperazine-2-carboxylate
CAS NO:1208321-05-4
Molecular Formula:
Molecular Weight: 461.561
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: tert-butyl 1,4-dimethyl-2-((2-methyl-1H-indol-3-yl)(phenyl)methyl)-3,6-dioxopiperazine-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl 1,4-dimethyl-2-((2-methyl-1H-indol-3-yl)(phenyl)methyl)-3,6-dioxopiperazine-2-carboxylate(1208321-05-4)
EPA Substance Registry System: tert-butyl 1,4-dimethyl-2-((2-methyl-1H-indol-3-yl)(phenyl)methyl)-3,6-dioxopiperazine-2-carboxylate(1208321-05-4)

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: 1208321-05-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1208321-05-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,3,2 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1208321-05:
(9*1)+(8*2)+(7*0)+(6*8)+(5*3)+(4*2)+(3*1)+(2*0)+(1*5)=104
104 % 10 = 4
So 1208321-05-4 is a valid CAS Registry Number.

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1208321-05-4Relevant academic research and scientific papers

Direct organocatalytic coupling of carboxylated piperazine-2,5-diones with indoles through conjugate addition of carbon nucleophiles to indolenine intermediates

Dubey, Ramin,Olenyuk, Bogdan

, p. 609 - 612 (2010)

Organocatalytic conjugate addition of diketopiperazines to indoles was achieved in good to excellent yields through electrophilic indolenine intermediates generated under mild conditions. Screening of catalysts and solvents at different temperatures was p

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