Cas 119841-80-4,3',4'-didemethoxy-4-deoxy-3',4'-dihydro-5-hydroxy-3',4'-dioxopodophyllotoxin

119841-80-4

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Basic information

Product Name: 3',4'-didemethoxy-4-deoxy-3',4'-dihydro-5-hydroxy-3',4'-dioxopodophyllotoxin
Synonyms: 3',4'-didemethoxy-4-deoxy-3',4'-dihydro-5-hydroxy-3',4'-dioxopodophyllotoxin
CAS NO:119841-80-4
Molecular Formula:
Molecular Weight: 384.342
EINECS: N/A
Product Categories: N/A
Mol File: 119841-80-4.mol
Article Data: 1

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: 3',4'-didemethoxy-4-deoxy-3',4'-dihydro-5-hydroxy-3',4'-dioxopodophyllotoxin(CAS DataBase Reference)
NIST Chemistry Reference: 3',4'-didemethoxy-4-deoxy-3',4'-dihydro-5-hydroxy-3',4'-dioxopodophyllotoxin(119841-80-4)
EPA Substance Registry System: 3',4'-didemethoxy-4-deoxy-3',4'-dihydro-5-hydroxy-3',4'-dioxopodophyllotoxin(119841-80-4)

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: 119841-80-4(Hazardous Substances Data)

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119841-80-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119841-80-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,4 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 119841-80:
(8*1)+(7*1)+(6*9)+(5*8)+(4*4)+(3*1)+(2*8)+(1*0)=144
144 % 10 = 4
So 119841-80-4 is a valid CAS Registry Number.

119841-80-4Upstream product

568-53-6 (5R,5aR,8aR)-10-Hydroxy-5-(4-hydroxy-3,5-dimethoxy-phenyl)-5,8,8a,9-tetrahydro-5aH-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6-one

119841-80-4Downstream Products

119841-80-4Relevant articles and documents

Lignans and Related Phenols. Part 18. The Synthesis of Quinones from Podophyllotoxin and its Analogues

Ayres, David C.,Ritchie, Timothy J.

, p. 2573 - 2578 (2007/10/02)

The preparation of quinones from podophyllotoxin and peltatins of the aryltetrahydronaphtalene class by oxidative demethylation is described.The derivation of 2'-substituted ortho-quinones from these products by the reductive addition of azide, bromide, a

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