569667-97-6 Usage
Molecular structure
A piperidine ring with a carboxylic acid group, a 3-chloro-2-oxopropyl group, and a Boc protecting group.
Molecular weight
295.77 g/mol
Appearance
A white crystalline solid
Solubility
Soluble in organic solvents such as ethanol, methanol, and acetonitrile, but insoluble in water.
Melting point
85-88°C
Boiling point
Not readily available due to its stability as a solid; however, it may decompose before reaching a boiling point.
Functional groups
Ester, Boc protecting group, and a chlorinated carbonyl group.
Reactivity
Boc-piperidine is relatively stable and does not readily react with other chemicals. However, it can be selectively removed under acidic or basic conditions to release the free amine.
Uses
Boc-piperidine is used as a protecting group for amines in organic synthesis, as a building block for the synthesis of pharmaceuticals and bioactive compounds, and in the production of polypeptides and peptides for research and pharmaceutical purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 569667-97-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,9,6,6 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 569667-97:
(8*5)+(7*6)+(6*9)+(5*6)+(4*6)+(3*7)+(2*9)+(1*7)=236
236 % 10 = 6
So 569667-97-6 is a valid CAS Registry Number.
569667-97-6Relevant academic research and scientific papers
Substituted aza indole compounds and salts thereof, composition and use thereof
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Paragraph 0458; 0460; 0461, (2018/11/03)
The invention provides a substituted azaindole compound having a structure as represented by a formula (I) and a pharmaceutically acceptable salt and a medicinal preparation thereof. The compound is used for adjusting activity of protein kinase and adjusting intercellular or intracellular signal response. The invention further relates to a pharmaceutical composition including the compound and a method of applying the pharmaceutical composition to treatment of highly proliferative diseases of mammals, especially of mankind.
Preparation of novel azabicyclic amines and α7 nicotinic acetylcholine receptor activity of derived aryl amides
Walker, Daniel P.,Acker, Brad A.,Jacobsen, E. Jon,Wishka, Donn G.
, p. 247 - 257 (2008/09/18)
(Chemical Equation Presented) Three new azabicyclic amines, namely exo-3-amino-1-azabicyclo[3.2.1]octane, 3-amino-1-azabicyclo-[3.2.2]nonane and exo-6-amino-8-azabicyclo[3.2.1]octane, have been designed and prepared as isosteres of 3-aminoquinuclidine. Ar
