Cas 251902-52-0,2-chloro-7-fluoro-6-methoxy-3-quinolinecarbaldehyde

251902-52-0

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Basic information

Product Name: 2-chloro-7-fluoro-6-methoxy-3-quinolinecarbaldehyde
Synonyms:
CAS NO:251902-52-0
Molecular Formula:
Molecular Weight: 239.633
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 383.3±37.0 °C(Predicted)
Flash Point: N/A
Appearance: N/A
Density: 1.421±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-chloro-7-fluoro-6-methoxy-3-quinolinecarbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 2-chloro-7-fluoro-6-methoxy-3-quinolinecarbaldehyde(251902-52-0)
EPA Substance Registry System: 2-chloro-7-fluoro-6-methoxy-3-quinolinecarbaldehyde(251902-52-0)

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: 251902-52-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 251902-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,9,0 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 251902-52:
(8*2)+(7*5)+(6*1)+(5*9)+(4*0)+(3*2)+(2*5)+(1*2)=120
120 % 10 = 0
So 251902-52-0 is a valid CAS Registry Number.

251902-52-0Upstream product

251902-52-0Downstream Products

251902-52-0Relevant academic research and scientific papers

SUBSTITUTED 6,7-DIALKOXY-3-ISOQUINOLINOL DERIVATIVES AS INHIBITORS OF PHOSPHODIESTERASE 10 (PDE10A)

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Page/Page column 87, (2012/09/05)

The invention relates to compounds of the formula wherein R′, R1, through R7 and Ar are as defined herein. These compounds are useful as inhibitors of phosphodiesterase 10 (PDE10A) which are useful in treating central nervous system diseases such as psychosis and also in treating, for example, obesity, type II diabetes, metabolic syndrome, glucose intolerance, pain and ophthalmic diseases.

Comptothecin analogues, preparation methods therefor, use thereof as drugs, and pharmaceutical compositions containing said analogues

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Example 72, (2008/06/13)

The compound of the formula wherein the substituents are defined as in the specification and its non-toxic, pharmaceutically acceptable salts which are useful for the treatment of viral infections, parasitic diseases and the treatment of cancer.

New tetracyclic analogues of camptothecins, their preparation processes, their use as medicaments and the pharmaceutical compositions containing them

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, (2008/06/13)

The invention relates to new tetracyclic analogues of camptothecin, their preparation processes, their use as medicaments and the pharmaceutical compositions containing them. Said analogues, which include in particular 3-hydroxy-3-(4-oxo-4,6-dihydroindoli

Homocamptothecins: Synthesis and antitumor activity of novel E-ring- modified camptothecin analogues

Lavergne, Olivier,Lesueur-Ginot, Laurence,Rodas, Francesc Pla,Kasprzyk, Philip G.,Pommier, Jacques,Demarquay, Danièle,Prévost, Grégoire,Ulibarri, Gérard,Rolland, Alain,Schiano-Liberatore, Anne-Marie,Harnett, Jeremiah,Pons, Dominique,Camara, José,Bigg, Dennis C. H.

, p. 5410 - 5419 (2007/10/03)

Homocamptothecin (hCPT), a camptothecin (CPT) analogue with a seven membered β-hydroxylactone which combines enhanced plasma stability and potent topoisomerase I (Topo I) mediated activity, is an attractive template for the elaboration of new anticancer a

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