Cas 92218-35-4,(2S,6S,13S)-3-Eth-(E)-ylidene-13-formyl-1,3,4,7,12,12b-hexahydro-2H,6H-2,6-methano-indolo[2,3-a]quinolizine-13-carboxylic acid methyl ester

92218-35-4

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Basic information

Product Name: (2S,6S,13S)-3-Eth-(E)-ylidene-13-formyl-1,3,4,7,12,12b-hexahydro-2H,6H-2,6-methano-indolo[2,3-a]quinolizine-13-carboxylic acid methyl ester
Synonyms:
CAS NO:92218-35-4
Molecular Formula:
Molecular Weight: 350.417
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: (2S,6S,13S)-3-Eth-(E)-ylidene-13-formyl-1,3,4,7,12,12b-hexahydro-2H,6H-2,6-methano-indolo[2,3-a]quinolizine-13-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,6S,13S)-3-Eth-(E)-ylidene-13-formyl-1,3,4,7,12,12b-hexahydro-2H,6H-2,6-methano-indolo[2,3-a]quinolizine-13-carboxylic acid methyl ester(92218-35-4)
EPA Substance Registry System: (2S,6S,13S)-3-Eth-(E)-ylidene-13-formyl-1,3,4,7,12,12b-hexahydro-2H,6H-2,6-methano-indolo[2,3-a]quinolizine-13-carboxylic acid methyl ester(92218-35-4)

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: 92218-35-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 92218-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,1 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92218-35:
(7*9)+(6*2)+(5*2)+(4*1)+(3*8)+(2*3)+(1*5)=124
124 % 10 = 4
So 92218-35-4 is a valid CAS Registry Number.

92218-35-4Upstream product

639-36-1 E-akuammidine

92218-35-4Downstream Products

92218-35-4Relevant academic research and scientific papers

Studies on Apocynaceae: Hemi-Synthesis of Vellosimine from Rhazine - Application of HOMCOR (COSY)-2D NMR Spectroscopy in Structure Eludication of Ajmaline-Sarpagine Skeleton

Banerji, J.,Das, B.,Chakrabarti, R.,Shoolery, J. N.

, p. 709 - 711 (2007/10/02)

The rare indole alkaloid vellosimine (1) has been isolated from Rauwolfia reflexa Teism and Binn.The occurrence of this indolic base has been observed for the first time in R. reflexa.The hemi-synthesis of this compound from rhazine has been achieved.The study of the HOMCOR (COSY)-2D NMR spectroscopy of vellosimine provides important information on structure of the alkaloids having ajmaline-sarpagine skeleton.

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