Cas 126935-07-7,9H-1,3-Dioxolo[4,5-b]xanthen-9-one, 5a,6,7,8,9a,10-hexahydro-5a-hydroxy-7,7-dimethyl-10-(3,4,5-trimethoxy phenyl)-

126935-07-7

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Basic information

Product Name: 9H-1,3-Dioxolo[4,5-b]xanthen-9-one, 5a,6,7,8,9a,10-hexahydro-5a-hydroxy-7,7-dimethyl-10-(3,4,5-trimethoxy phenyl)-
Synonyms:
CAS NO:126935-07-7
Molecular Formula: C25H28O8
Molecular Weight: 456.493
EINECS: N/A
Product Categories: N/A
Mol File: 126935-07-7.mol

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: 9H-1,3-Dioxolo[4,5-b]xanthen-9-one, 5a,6,7,8,9a,10-hexahydro-5a-hydroxy-7,7-dimethyl-10-(3,4,5-trimethoxy phenyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 9H-1,3-Dioxolo[4,5-b]xanthen-9-one, 5a,6,7,8,9a,10-hexahydro-5a-hydroxy-7,7-dimethyl-10-(3,4,5-trimethoxy phenyl)-(126935-07-7)
EPA Substance Registry System: 9H-1,3-Dioxolo[4,5-b]xanthen-9-one, 5a,6,7,8,9a,10-hexahydro-5a-hydroxy-7,7-dimethyl-10-(3,4,5-trimethoxy phenyl)-(126935-07-7)

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: 126935-07-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126935-07-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,9,3 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 126935-07:
(8*1)+(7*2)+(6*6)+(5*9)+(4*3)+(3*5)+(2*0)+(1*7)=137
137 % 10 = 7
So 126935-07-7 is a valid CAS Registry Number.

126935-07-7Upstream product

126935-07-7Downstream Products

126935-07-7Relevant academic research and scientific papers

Synthesis of new benzopyrans related to podophyllotoxin

Jurd

, p. 1349 - 1352 (2007/10/02)

Mannich bases of types 1 or 8, which are readily synthesized by condensation of 3,4-methylenedioxyphenol with aromatic aldehydes and pyrrolidine or piperazine, react with cyclic and acyclic β-diketones to yield benzopyrans. These benzopyrans are structurally similar to podophyllotoxin and like this drug some of the benzopyrans show in vivo anti-leukemic action in mice.

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