201478-72-0 Usage
Description
3-Formyl-piperidine-1-carboxylic Acid Benzyl Ester is a chemical compound that belongs to the class of organic compounds known as aryl-aliphatic ketones. It is predominantly used in the field of organic chemistry as an intermediate due to its reactive carbonyl group. The molecular structure of this compound includes a piperidine ring, which is a six-membered ring with one nitrogen atom, a benzyl ester group, and a formyl group. The chemical formula for this compound is C16H19NO3. Although its properties like toxicity and biological activity are not widely studied or reported, its reactions and transformations are significant in the synthesis of more complex chemicals within the pharmaceutical and chemical industries.
Uses
Used in Organic Chemistry:
3-Formyl-piperidine-1-carboxylic Acid Benzyl Ester is used as a chemical intermediate for the synthesis of more complex chemicals. Its reactive carbonyl group allows for various reactions and transformations, making it a valuable component in the development of new compounds.
Used in Pharmaceutical Industry:
3-Formyl-piperidine-1-carboxylic Acid Benzyl Ester is used as a building block in the synthesis of pharmaceutical compounds. Its unique molecular structure, including the piperidine ring, benzyl ester group, and formyl group, contributes to the creation of novel drug molecules with potential therapeutic applications.
Used in Chemical Industry:
3-Formyl-piperidine-1-carboxylic Acid Benzyl Ester is used as a key component in the production of specialty chemicals. Its versatility in undergoing various chemical reactions enables the creation of a wide range of chemical products for different applications, such as materials science, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 201478-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,4,7 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 201478-72:
(8*2)+(7*0)+(6*1)+(5*4)+(4*7)+(3*8)+(2*7)+(1*2)=110
110 % 10 = 0
So 201478-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO3/c16-10-13-7-4-8-15(9-13)14(17)18-11-12-5-2-1-3-6-12/h1-3,5-6,10,13H,4,7-9,11H2
201478-72-0Relevant articles and documents
Potent inhibition of Norwalk virus by cyclic sulfamide derivatives
Dou, Dengfeng,Tiew, Kok-Chuan,He, Guijia,Mandadapu, Sivakoteswara Rao,Aravapalli, Sridhar,Alliston, Kevin R.,Kim, Yunjeong,Chang, Kyeong-Ok,Groutas, William C.
, p. 5975 - 5983 (2011/11/07)
A new class of compounds that exhibit anti-norovirus activity in a cell-based system and embody in their structure a cyclosulfamide scaffold has been identified. The structure of the initial hit (compound 2a, ED50 4 μM, TD50 50 μM) has been prospected by exploiting multiple points of diversity and generating appropriate structure-activity relationships.
Disubstituted pyrimidines as Lck inhibitors
Hunt, Julianne A.,Beresis, Richard T.,Goulet, Joung L.,Holmes, Mark A.,Hong, Xinfang J.,Kovacs, Ernest,Mills, Sander G.,Ruzek, Rowena D.,Wong, Frederick,Hermes, Jeffrey D.,Park, Young-Whan,Salowe, Scott P.,Sonatore, Lisa M.,Wu, Lin,Woods, Andrea,Zaller, Dennis M.,Sinclair, Peter J.
supporting information; scheme or table, p. 5440 - 5443 (2010/04/26)
We have developed a family of 4-benzimidazolyl-N-piperazinethyl-pyrimidin-2-amines that are subnanomolar inhibitors of Lck. A subset of these Lck inhibitors, with heterocyclic substituents at the benzimidazole C5, are also low-nanomolar inhibitors of cell
Pyridine derivatives
-
, (2008/06/13)
Pyridine compounds of general formula: wherein —R1represents in which R11is hydrogen, C1-6alkyl, halogen, hydroxy, C1-12alkoxy, nitro, amino, C1-6alkylsulfonylamino, C1-6alkoxycarbonyl, C1-6alkylamino, di(C1-6alkyl)amino, C1-6alkanoylamino, phenyl C1-6alkylamino, phenylsulfonylamino, or —O—(CH2)n—R111; R2represents hydrogen or halogen; R3represents hydrogen, —CR31R32R33, or —NR34R35; R4is hydrogen, carbamoyl, CN, carboxyl, etc.; R5is amino, C1-6alkylamino, di C1-6alkylamino, etc. or salt thereof. The compound has an excellent anti-inflammatory activity, and other biological activity.
