Cas 1223487-79-3,(13aS,14S)-14-hydroxy-6,7-dimethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinolin-3-yl prop-2-yn-1-yl carbonate

1223487-79-3

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Basic information

Product Name: (13aS,14S)-14-hydroxy-6,7-dimethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinolin-3-yl prop-2-yn-1-yl carbonate
Synonyms: (13aS,14S)-14-hydroxy-6,7-dimethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinolin-3-yl prop-2-yn-1-yl carbonate
CAS NO:1223487-79-3
Molecular Formula:
Molecular Weight: 447.488
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: (13aS,14S)-14-hydroxy-6,7-dimethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinolin-3-yl prop-2-yn-1-yl carbonate(CAS DataBase Reference)
NIST Chemistry Reference: (13aS,14S)-14-hydroxy-6,7-dimethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinolin-3-yl prop-2-yn-1-yl carbonate(1223487-79-3)
EPA Substance Registry System: (13aS,14S)-14-hydroxy-6,7-dimethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinolin-3-yl prop-2-yn-1-yl carbonate(1223487-79-3)

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: 1223487-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1223487-79-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,3,4,8 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1223487-79:
(9*1)+(8*2)+(7*2)+(6*3)+(5*4)+(4*8)+(3*7)+(2*7)+(1*9)=153
153 % 10 = 3
So 1223487-79-3 is a valid CAS Registry Number.

1223487-79-3Upstream product

35718-08-2 propargyl chloroformate

1223487-79-3Downstream Products

1223487-79-3Relevant academic research and scientific papers

Synthesis of phenanthroindolizidine alkaloids with an acyloxy group at the C3 position and their antitumor activities and toxicities

Ikeda, Takashi,Yaegashi, Takashi,Matsuzaki, Takeshi,Yamazaki, Ryuta,Ueno, Satoshi,Hashimoto, Syusuke,Sawada, Seigo

, p. 447 - 453 (2012)

We previously reported that the phenanthroindolizidine alkaloid 3 and its derivatives had markedly potent in vitro cytotoxicity. However, they had low in vivo antitumor activities and high in vivo toxicities, which was a serious problem for further develo

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