Cas 1026224-01-0,Benzoic acid (1S,2S,9R,10R)-1,4-dihydroxy-9-(2-hydroxy-ethoxy)-12,15,15-trimethyl-13-oxo-10-phenylsulfanyl-tricyclo[9.3.1.0<sup>3,8</sup>]pentadeca-3<sup>(8)</sup>,4,6,11-tetraen-2-yl ester

1026224-01-0

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Basic information

Product Name: Benzoic acid (1S,2S,9R,10R)-1,4-dihydroxy-9-(2-hydroxy-ethoxy)-12,15,15-trimethyl-13-oxo-10-phenylsulfanyl-tricyclo[9.3.1.0^3,8]pentadeca-3⁽⁸⁾,4,6,11-tetraen-2-yl ester
Synonyms:
CAS NO:1026224-01-0
Molecular Formula:
Molecular Weight: 574.695
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: Benzoic acid (1S,2S,9R,10R)-1,4-dihydroxy-9-(2-hydroxy-ethoxy)-12,15,15-trimethyl-13-oxo-10-phenylsulfanyl-tricyclo[9.3.1.0^3,8]pentadeca-3⁽⁸⁾,4,6,11-tetraen-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (1S,2S,9R,10R)-1,4-dihydroxy-9-(2-hydroxy-ethoxy)-12,15,15-trimethyl-13-oxo-10-phenylsulfanyl-tricyclo[9.3.1.0^3,8]pentadeca-3⁽⁸⁾,4,6,11-tetraen-2-yl ester(1026224-01-0)
EPA Substance Registry System: Benzoic acid (1S,2S,9R,10R)-1,4-dihydroxy-9-(2-hydroxy-ethoxy)-12,15,15-trimethyl-13-oxo-10-phenylsulfanyl-tricyclo[9.3.1.0^3,8]pentadeca-3⁽⁸⁾,4,6,11-tetraen-2-yl ester(1026224-01-0)

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: 1026224-01-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1026224-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,2,2 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1026224-01:
(9*1)+(8*0)+(7*2)+(6*6)+(5*2)+(4*2)+(3*4)+(2*0)+(1*1)=90
90 % 10 = 0
So 1026224-01-0 is a valid CAS Registry Number.

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1026224-01-0Relevant 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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