Cas 522664-87-5,4-PiperidineMethanaMine, 1-[(tetrahydro-2H-pyran-4-yl)Methyl]-

522664-87-5

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Basic information

Product Name: 4-PiperidineMethanaMine, 1-[(tetrahydro-2H-pyran-4-yl)Methyl]-
Synonyms: 4-PiperidineMethanaMine, 1-[(tetrahydro-2H-pyran-4-yl)Methyl]-;[1-(oxan-4-ylmethyl)piperidin-4-yl]methanamine
CAS NO:522664-87-5
Molecular Formula: C₁₂H₂₄N₂O
Molecular Weight: 212.33176
EINECS: N/A
Product Categories: N/A
Mol File: 522664-87-5.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 317.6±7.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 0.995±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 10.13±0.29(Predicted)
CAS DataBase Reference: 4-PiperidineMethanaMine, 1-[(tetrahydro-2H-pyran-4-yl)Methyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 4-PiperidineMethanaMine, 1-[(tetrahydro-2H-pyran-4-yl)Methyl]-(522664-87-5)
EPA Substance Registry System: 4-PiperidineMethanaMine, 1-[(tetrahydro-2H-pyran-4-yl)Methyl]-(522664-87-5)

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: 522664-87-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 522664-87-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,2,6,6 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 522664-87:
(8*5)+(7*2)+(6*2)+(5*6)+(4*6)+(3*4)+(2*8)+(1*7)=155
155 % 10 = 5
So 522664-87-5 is a valid CAS Registry Number.

522664-87-5Upstream product

522664-87-5Downstream Products

522664-87-5Relevant academic research and scientific papers

Process for the preparation of ibodutant (MEN15596) and related intermediates

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Page/Page column 12, (2013/05/09)

This invention relates to a novel process for synthesizing the product ibodutant shown in the figure below, consisting of a small number of high-yield steps involving reagents and solvents with low environmental impact, characterized by the coupling of two portions, compounds (3) and (4), one of which (3) is synthesized by coupling of 6-methyl-2-benzo[b]thiophenecarboxylic acid (1) with 1-amino-alpha-alpha-cyclopentan carboxylic acid and subsequent cyclization with oxazolone, while the other, compound (4), is obtained from suitable highly selective functionalizations of 4-aminomethylpiperidine (2).

PROCESS FOR THE PREPARATION OF IBODUTANT (MEN15596) AND RELATED INTERMEDIATES

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Page/Page column 8; 13; 14, (2010/12/18)

This invention relates to a novel process for synthesising the product ibodutant shown in the figure below, consisting of a small number of high- yield steps involving reagents and solvents with low environmental impact, characterised by the coupling of two portions, compounds (3) and (4), one of which (3) is synthesised by coupling of 6-methyl-2- benzo[b]thiophenecarboxylic acid (1) with 1-amino-alpha-alpha-cyclopentan carboxylic acid and subsequent cyclization with oxazolone, while the other, compound (4), is obtained from suitable highly selective functionalisations of 4-aminomethylpiperidine (2).

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