Cas 1290047-24-3,ethyl [(-6-oxo-5-(2-phenylethyl)-4,5,6,7-tetrahydro-3,5,7a-triazacyclohepta[jk]fluoren-4-ylcarbonyl)amino]acetate

1290047-24-3

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Basic information

Product Name: ethyl [(-6-oxo-5-(2-phenylethyl)-4,5,6,7-tetrahydro-3,5,7a-triazacyclohepta[jk]fluoren-4-ylcarbonyl)amino]acetate
Synonyms:
CAS NO:1290047-24-3
Molecular Formula:
Molecular Weight: 470.528
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: ethyl [(-6-oxo-5-(2-phenylethyl)-4,5,6,7-tetrahydro-3,5,7a-triazacyclohepta[jk]fluoren-4-ylcarbonyl)amino]acetate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl [(-6-oxo-5-(2-phenylethyl)-4,5,6,7-tetrahydro-3,5,7a-triazacyclohepta[jk]fluoren-4-ylcarbonyl)amino]acetate(1290047-24-3)
EPA Substance Registry System: ethyl [(-6-oxo-5-(2-phenylethyl)-4,5,6,7-tetrahydro-3,5,7a-triazacyclohepta[jk]fluoren-4-ylcarbonyl)amino]acetate(1290047-24-3)

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: 1290047-24-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1290047-24-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,0,0,4 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1290047-24:
(9*1)+(8*2)+(7*9)+(6*0)+(5*0)+(4*4)+(3*7)+(2*2)+(1*4)=133
133 % 10 = 3
So 1290047-24-3 is a valid CAS Registry Number.

1290047-24-3Upstream product

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1290047-24-3Relevant academic research and scientific papers

Convenient synthesis of a library of lactam-fused β-carbolines via the Ugi reaction

Hutait, Samiran,Nayak, Maloy,Penta, Ashok,Batra, Sanjay

experimental part, p. 419 - 430 (2011/04/15)

We present a convenient synthesis of a chemical library of lactam-fused β-carbolines via a Ugi four-center three-component reaction employing [1-formyl-3-(methoxycarbonyl)-9H-pyrido[3,4-b]indol-9-yl]acetic acid or (1-formyl-9H-pyrido[3,4-b]indol-9-yl)acet

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