Cas 1073610-31-7,4β-[4-(1,3-benzothiazole-2-yl)anilino]-4-desoxypodophyllotoxin

1073610-31-7

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Basic information

Product Name: 4β-[4-(1,3-benzothiazole-2-yl)anilino]-4-desoxypodophyllotoxin
Synonyms: 4β-[4-(1,3-benzothiazole-2-yl)anilino]-4-desoxypodophyllotoxin
CAS NO:1073610-31-7
Molecular Formula:
Molecular Weight: 622.698
EINECS: N/A
Product Categories: N/A
Mol File: 1073610-31-7.mol
Article Data: 2

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: 4β-[4-(1,3-benzothiazole-2-yl)anilino]-4-desoxypodophyllotoxin(CAS DataBase Reference)
NIST Chemistry Reference: 4β-[4-(1,3-benzothiazole-2-yl)anilino]-4-desoxypodophyllotoxin(1073610-31-7)
EPA Substance Registry System: 4β-[4-(1,3-benzothiazole-2-yl)anilino]-4-desoxypodophyllotoxin(1073610-31-7)

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: 1073610-31-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1073610-31-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,6,1 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1073610-31:
(9*1)+(8*0)+(7*7)+(6*3)+(5*6)+(4*1)+(3*0)+(2*3)+(1*1)=117
117 % 10 = 7
So 1073610-31-7 is a valid CAS Registry Number.

1073610-31-7Upstream product

6278-73-5 2-(4-aminophenyl)benzothiazole

1073610-31-7Downstream Products

1073610-31-7Relevant articles and documents

An efficient one-pot synthesis of benzothiazolo-4β-anilino- podophyllotoxin congeners: DNA topoisomerase-II inhibition and anticancer activity

Kamal, Ahmed,Kumar, B. Ashwini,Suresh, Paidakula,Shankaraiah, Nagula,Kumar, M. Shiva

experimental part, p. 350 - 353 (2011/02/27)

An efficient one-pot iodination methodology for the synthesis of benzothiazolo-4β-anilino-podophyllotoxin (5a-h) and benzothiazolo-4β- anilino-4-O-demethylepipodophyllotoxin (6a-h) congeners has been successfully developed by using zirconium tetrachloride

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