Cas 219523-50-9,(1S,2S,9R,10R)-1,2-Dihydroxy-9-(2-hydroxy-ethoxy)-4-methoxy-12,15,15-trimethyl-10-phenylsulfanyl-tricyclo[9.3.1.0<sup>3,8</sup>]pentadeca-3<sup>(8)</sup>,4,6,11-tetraen-13-one

219523-50-9

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Basic information

Product Name: (1S,2S,9R,10R)-1,2-Dihydroxy-9-(2-hydroxy-ethoxy)-4-methoxy-12,15,15-trimethyl-10-phenylsulfanyl-tricyclo[9.3.1.0^3,8]pentadeca-3⁽⁸⁾,4,6,11-tetraen-13-one
Synonyms:
CAS NO:219523-50-9
Molecular Formula:
Molecular Weight: 484.613
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: (1S,2S,9R,10R)-1,2-Dihydroxy-9-(2-hydroxy-ethoxy)-4-methoxy-12,15,15-trimethyl-10-phenylsulfanyl-tricyclo[9.3.1.0^3,8]pentadeca-3⁽⁸⁾,4,6,11-tetraen-13-one(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,9R,10R)-1,2-Dihydroxy-9-(2-hydroxy-ethoxy)-4-methoxy-12,15,15-trimethyl-10-phenylsulfanyl-tricyclo[9.3.1.0^3,8]pentadeca-3⁽⁸⁾,4,6,11-tetraen-13-one(219523-50-9)
EPA Substance Registry System: (1S,2S,9R,10R)-1,2-Dihydroxy-9-(2-hydroxy-ethoxy)-4-methoxy-12,15,15-trimethyl-10-phenylsulfanyl-tricyclo[9.3.1.0^3,8]pentadeca-3⁽⁸⁾,4,6,11-tetraen-13-one(219523-50-9)

Safety Data

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Statements: N/A
Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 219523-50-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 219523-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,5,2 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 219523-50:
(8*2)+(7*1)+(6*9)+(5*5)+(4*2)+(3*3)+(2*5)+(1*0)=129
129 % 10 = 9
So 219523-50-9 is a valid CAS Registry Number.

219523-50-9Upstream product

219523-50-9Downstream Products

219523-54-3 C₄₁H₄₀O₈S

219523-50-9Relevant academic research and scientific papers

Synthesis of C-ring aromatic taxoids and evaluation of their multi-drug resistance reversing activity

Morihira, Koichiro,Nishimori, Toshiyuki,Kusama, Hiroyuki,Horiguchi, Yoshiaki,Kuwajima, Isao,Tsuruo, Takashi

, p. 2973 - 2976 (2007/10/03)

The C-aromatic taxoids were synthesized to develop effective inhibitors against drug efflux mediated by p-glycoproteins. Among those tested using multi-drug resistant tumor cells (2780AD), the benzoate 11 exhibited significant activity as potent as verapa

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