Cas 324575-73-7,7-Azabicyclo[2.2.1]heptane,2-(4-pyridazinyl)-,(1R,2R,4S)-rel-(9CI)

324575-73-7

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Basic information

Product Name: 7-Azabicyclo[2.2.1]heptane,2-(4-pyridazinyl)-,(1R,2R,4S)-rel-(9CI)
Synonyms: 7-Azabicyclo[2.2.1]heptane,2-(4-pyridazinyl)-,(1R,2R,4S)-rel-(9CI)
CAS NO:324575-73-7
Molecular Formula: C10H13N3
Molecular Weight: 175.23032
EINECS: N/A
Product Categories: CYCLOHEXANE
Mol File: 324575-73-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 7-Azabicyclo[2.2.1]heptane,2-(4-pyridazinyl)-,(1R,2R,4S)-rel-(9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 7-Azabicyclo[2.2.1]heptane,2-(4-pyridazinyl)-,(1R,2R,4S)-rel-(9CI)(324575-73-7)
EPA Substance Registry System: 7-Azabicyclo[2.2.1]heptane,2-(4-pyridazinyl)-,(1R,2R,4S)-rel-(9CI)(324575-73-7)

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: 324575-73-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 324575-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,4,5,7 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 324575-73:
(8*3)+(7*2)+(6*4)+(5*5)+(4*7)+(3*5)+(2*7)+(1*3)=147
147 % 10 = 7
So 324575-73-7 is a valid CAS Registry Number.

324575-73-7Upstream product

324575-73-7Downstream Products

324575-73-7Relevant academic research and scientific papers

exo-2-(pyridazin-4-yl)-7-azabicyclo[2.2.1]heptanes: Syntheses and nicotinic acetylcholine receptor agonist activity of potent pyridazine analogues of (±)-epibatidine

Che,Wegge,Stubbs,Seitz,Meier,Methfessel

, p. 47 - 57 (2007/10/03)

A new strategy for the straightforward synthesis of novel racemic epibatidine analogues is presented, in which the 2-chloropyridinyl moiety of epibatidine is bioisosterically replaced by differently substituted pyridazine rings. A key step of the new synt

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