Cas 1313356-78-3,6-fluoro-2-(3-methoxyphenyl)quinolin-4-yl 3,4,5-trimethoxybenzenesulfonate

1313356-78-3

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Basic information

Product Name: 6-fluoro-2-(3-methoxyphenyl)quinolin-4-yl 3,4,5-trimethoxybenzenesulfonate
Synonyms: 6-fluoro-2-(3-methoxyphenyl)quinolin-4-yl 3,4,5-trimethoxybenzenesulfonate
CAS NO:1313356-78-3
Molecular Formula:
Molecular Weight: 499.517
EINECS: N/A
Product Categories: N/A
Mol File: 1313356-78-3.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: 6-fluoro-2-(3-methoxyphenyl)quinolin-4-yl 3,4,5-trimethoxybenzenesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: 6-fluoro-2-(3-methoxyphenyl)quinolin-4-yl 3,4,5-trimethoxybenzenesulfonate(1313356-78-3)
EPA Substance Registry System: 6-fluoro-2-(3-methoxyphenyl)quinolin-4-yl 3,4,5-trimethoxybenzenesulfonate(1313356-78-3)

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: 1313356-78-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1313356-78-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,3,5 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1313356-78:
(9*1)+(8*3)+(7*1)+(6*3)+(5*3)+(4*5)+(3*6)+(2*7)+(1*8)=133
133 % 10 = 3
So 1313356-78-3 is a valid CAS Registry Number.

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1313356-78-3Relevant articles and documents

Novel 2-Substituted quinolin-4-yl-benzenesulfonate derivatives: Synthesis, antiproliferative activity, and inhibition of cellular tubulin polymerization

Kakadiya, Rajesh,Wu, Yi-Chen,Dong, Huajin,Kuo, Hsiao-Hui,Yih, Ling-Huei,Chou, Ting-Chao,Su, Tsann-Long

experimental part, p. 1119 - 1129 (2012/01/06)

A series of 2-substituted quinolin-4-yl-benzenesulfonate derivatives were synthesized for the purpose of evaluating antiproliferative activity. Structure-activity relationships of the newly synthesized compounds against human lymphoblastic leukemia and va

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