167262-92-2 Usage
Molecular structure
Piperidine derivative with a BOC protecting group, a cyano group, and a pyridinyl group attached to the piperidine ring
Functional groups
BOC (tert-butyloxycarbonyl), cyano (-CN), and pyridinyl (C5H4N)
Appearance
Unknown, but likely a solid or crystalline substance
Solubility
Unknown, but may be soluble in organic solvents like methanol, ethanol, or acetone
Stability
Stable under normal conditions, but sensitive to hydrolysis or other reactions that could remove the BOC protecting group
Reactivity
Reacts with various reagents to form new compounds, particularly in organic synthesis and pharmaceutical applications
Applications
Building block in organic synthesis, used in the pharmaceutical industry for drug production, and as a research chemical for developing new compounds with potential pharmacological activities
Importance
Versatile compound in organic chemistry and drug discovery, contributing to the development of various drugs and pharmaceuticals
Safety
Potential hazards and safety precautions not provided, but should be handled with care due to its reactivity and potential use in pharmaceuticals
Check Digit Verification of cas no
The CAS Registry Mumber 167262-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,2,6 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 167262-92:
(8*1)+(7*6)+(6*7)+(5*2)+(4*6)+(3*2)+(2*9)+(1*2)=152
152 % 10 = 2
So 167262-92-2 is a valid CAS Registry Number.
167262-92-2Relevant articles and documents
Preparation of 4-heteroaryl-4-cyanopiperidines via SNAr substitution reactions
Chang, Ronald K.,Di Marco, Christina N.,Pitts, Daniel R.,Greshock, Thomas J.,Kuduk, Scott D.
, p. 6303 - 6306 (2009)
The scope and limitations of SNAr substitution reactions of metalated 4-cyanopiperidines with heterocyclic halides were explored. These facile reactions provide rapid access to a wide range of 4-heteroaryl-4-cyanopiperidines and have resulted i
THIAZOLYL COMPOUNDS USEFUL AS KINASE INHIBITORS
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Page/Page column 63, (2008/12/04)
The invention provides compounds of formula (I) and pharmaceutically acceptable salts thereof. The formula I thiazolyl compounds inhibit tyrosine kinase activity thereby making them useful as anticancer agents and for the treatment of Alzheimer's disease
SUBSTITUTED PYRROLIDIN-3-YL-ALKYL-PIPERIDINES
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, (2008/06/13)
The present invention relates to substituted pyrrolidinyl-3-yl-alkyl-piperidines, their stereoisomers, and pharmaceutically acceptable salts thereof and processes for preparation of the same. The compounds of the present invention are useful in their pharmacological activities such as tachykinin antagonism, especially substance P and neurokinin A antagonism, and the like. Compounds having the property of tachykinin antagonism are indicated for conditions associated with neurogenic inflammation and other diseases described herein.
