Cas 523-08-0,(7aR,8S,10R,11aR,12aS)-8-Methyl-5,6,7a,8,10,11,11a,12,12a,13-decahydro-7H-9-oxa-6a,13-diaza-indeno[2,1-a]anthracen-10-ol

523-08-0

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Basic information

Product Name: (7aR,8S,10R,11aR,12aS)-8-Methyl-5,6,7a,8,10,11,11a,12,12a,13-decahydro-7H-9-oxa-6a,13-diaza-indeno[2,1-a]anthracen-10-ol
Synonyms:
CAS NO:523-08-0
Molecular Formula:
Molecular Weight: 312.412
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: (7aR,8S,10R,11aR,12aS)-8-Methyl-5,6,7a,8,10,11,11a,12,12a,13-decahydro-7H-9-oxa-6a,13-diaza-indeno[2,1-a]anthracen-10-ol(CAS DataBase Reference)
NIST Chemistry Reference: (7aR,8S,10R,11aR,12aS)-8-Methyl-5,6,7a,8,10,11,11a,12,12a,13-decahydro-7H-9-oxa-6a,13-diaza-indeno[2,1-a]anthracen-10-ol(523-08-0)
EPA Substance Registry System: (7aR,8S,10R,11aR,12aS)-8-Methyl-5,6,7a,8,10,11,11a,12,12a,13-decahydro-7H-9-oxa-6a,13-diaza-indeno[2,1-a]anthracen-10-ol(523-08-0)

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: 523-08-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 523-08-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 523-08:
(5*5)+(4*2)+(3*3)+(2*0)+(1*8)=50
50 % 10 = 0
So 523-08-0 is a valid CAS Registry Number.

523-08-0Upstream product

483-04-5 ajmalicine

523-08-0Downstream Products

523-08-0Relevant academic research and scientific papers

Heteroyohimbine Alkaloids. Stereospecific Conversion of Ajmalicine into 19-Epiajmalicine

Palmisano, Giovanni,Danieli, Bruno,Lesma, Giordano,Riva, Renata

, p. 923 - 926 (2007/10/02)

An efficient four-step sequence to 19-epiajmalicine, a rare heteroyohimbane alkaloid, which requires mild conditions and utilises ajmalicine as an easily accessible starting material, is described.

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