214548-40-0 Usage
Ester derivative
1-Piperidinecarboxylic acid, 3-(hydroxymethyl)-, ethyl ester is an ester derivative of 3-(hydroxymethyl)piperidinecarboxylic acid, meaning it has an ester functional group attached to the piperidine ring.
Pharmaceutical industry use
This compound is often used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical compounds, indicating its importance in creating new drugs and therapies.
Potential applications
1-Piperidinecarboxylic acid, 3-(hydroxymethyl)-, ethyl ester has potential applications in the development of drugs and other bioactive molecules, suggesting that it may be useful in creating new treatments and medications.
Unique chemical structure and reactivity
The compound has a unique chemical structure and reactivity, which contributes to its potential applications in drug development and synthesis.
Safety precautions
It is important to handle 1-Piperidinecarboxylic acid, 3-(hydroxymethyl)-, ethyl ester with care and follow proper safety protocols, as it can pose potential hazards if mishandled, indicating that proper handling and storage procedures are necessary to prevent accidents and ensure safe use.
Check Digit Verification of cas no
The CAS Registry Mumber 214548-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,5,4 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 214548-40:
(8*2)+(7*1)+(6*4)+(5*5)+(4*4)+(3*8)+(2*4)+(1*0)=120
120 % 10 = 0
So 214548-40-0 is a valid CAS Registry Number.
214548-40-0Relevant articles and documents
Novel compounds useful for bradykinin B1 receptor antagonism
-
Page/Page column 42, (2010/11/25)
Disclosed are compounds that are bradykinin B1 receptor antagonists and are useful for treating diseases, or relieving adverse symptoms associated with disease conditions, in mammals mediated by bradykinin B1 receptor.
Synthesis of racemic nitramine, isonitramine and sibirine
Deyine, Abdallah,Poirier, Jean-Marie,Duhamel, Lucette,Duhamel, Pierre
, p. 2491 - 2493 (2007/10/03)
Condensation of enol ether 6 with methyl vinyl ketone led easily to ketoaldehyde 7 whose cyclisation afforded the azaspiranic enone 8, a key intermediate for the synthesis of the title alkaloids.
1,2,3,4-tetrahydro-benzofuro[3,2-C]pyridine derivatives
-
, (2008/06/13)
PCT No. PCT/EP98/02136 Sec. 371 Date Oct. 4, 1999 Sec. 102(e) Date Oct. 4, 1999 PCT Filed Apr. 2, 1998 PCT Pub. No. WO98/45297 PCT Pub. Date Oct. 15, 1998The present invention concerns the compounds of formula the N-oxides, the pharmaceutically acceptable