Cas 858355-21-2,4-benzoyl-8-carbethoxy-10-methyl-4,5a,6,7,9,10a-dodecahydro-Δ<sup>10β</sup>-dehydroindolo<3,4-gh>quinoline

858355-21-2

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Basic information

Product Name: 4-benzoyl-8-carbethoxy-10-methyl-4,5a,6,7,9,10a-dodecahydro-Δ^10β-dehydroindolo<3,4-gh>quinoline
Synonyms: 4-benzoyl-8-carbethoxy-10-methyl-4,5a,6,7,9,10a-dodecahydro-Δ^10β-dehydroindolo<3,4-gh>quinoline
CAS NO:858355-21-2
Molecular Formula:
Molecular Weight: 404.509
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: 4-benzoyl-8-carbethoxy-10-methyl-4,5a,6,7,9,10a-dodecahydro-Δ^10β-dehydroindolo<3,4-gh>quinoline(CAS DataBase Reference)
NIST Chemistry Reference: 4-benzoyl-8-carbethoxy-10-methyl-4,5a,6,7,9,10a-dodecahydro-Δ^10β-dehydroindolo<3,4-gh>quinoline(858355-21-2)
EPA Substance Registry System: 4-benzoyl-8-carbethoxy-10-methyl-4,5a,6,7,9,10a-dodecahydro-Δ^10β-dehydroindolo<3,4-gh>quinoline(858355-21-2)

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: 858355-21-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 858355-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,3,5 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 858355-21:
(8*8)+(7*5)+(6*8)+(5*3)+(4*5)+(3*5)+(2*2)+(1*1)=202
202 % 10 = 2
So 858355-21-2 is a valid CAS Registry Number.

858355-21-2Upstream product

1027020-87-6 4-benzoyl-8-carbethoxy-10-methyl-4,5a,6,7,9,10a-dodecahydro-Δ^6αΔ^10β-didehydroindolo<3,4-gh>quinoline

858355-21-2Downstream Products

858355-21-2Relevant academic research and scientific papers

Synthesis and analysis of compounds having the skeleton of ergot alkaloids with the nitrogen atom in the D-ring transposed

Stamos,Kelly,Floss,Cassady

, p. 1303 - 1308 (2007/10/03)

Alkylation-amination of the enamine 2 in the presence of ethyl α,α-bis(dibromomethyl)acetate, triethylamine, and methylamine lead to the construction of the aza-transposed ergoline 3. Sequential reduction, hydrolysis, reesterification, and indolization of

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