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CAS

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1217977-05-3

(S)-1-Cbz-3-(aminomethyl)piperidine, also known as (S)-3-(aminomethyl)piperidine-1-carboxylic acid benzyl ester, is a piperidine derivative with a molecular formula of C14H21N2O and a molecular weight of 231.33 g/mol. It features a benzyl ester group attached to the carboxylic acid functional group and an aminoalkyl substituent on the piperidine ring. This chiral building block is widely used in the pharmaceutical industry for the synthesis of various pharmaceutical compounds and as a key component in organic chemistry.

1217977-05-3

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1217977-05-3 Usage

Uses

Used in Pharmaceutical Industry:
(S)-1-Cbz-3-(aminomethyl)piperidine is used as a chiral building block for the synthesis of various pharmaceutical compounds. Its unique structure and functional groups enable the development of new drugs with improved efficacy and selectivity.
Used in Organic Chemistry:
In the field of organic chemistry, (S)-1-Cbz-3-(aminomethyl)piperidine serves as a valuable building block for the synthesis of complex organic molecules. Its versatile structure allows for further functionalization and modification, facilitating the creation of novel compounds with potential applications in various industries.
Used in Medicinal Applications:
(S)-1-Cbz-3-(aminomethyl)piperidine has potential medicinal applications due to its unique structure and functional groups. It can be incorporated into drug molecules to enhance their pharmacological properties, such as potency, selectivity, and bioavailability.

Check Digit Verification of cas no

The CAS Registry Mumber 1217977-05-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,9,7 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1217977-05:
(9*1)+(8*2)+(7*1)+(6*7)+(5*9)+(4*7)+(3*7)+(2*0)+(1*5)=173
173 % 10 = 3
So 1217977-05-3 is a valid CAS Registry Number.

1217977-05-3Upstream product

1217977-05-3Downstream Products

1217977-05-3Relevant articles and documents

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

NOVEL COMPOUNDS WITH ANTIBACTERIAL ACTIVITY

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Page/Page column 17-18, (2010/02/06)

The invention relates to novel antibacterial compounds of formula (I).

SRC kinase inhibitor compounds

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, (2008/06/13)

Pyrimidine compounds (Formula I), or their pharmaceutically acceptable salts, hydrates, solvates, crystal forms and individual diastereomers, and pharmaceutical compositions including the same, which are inhibitors of tyrosine kinase enzymes, and as such are useful in the prophylaxis and treatment of proteins tyrosine kinase-associated disorders, such as immune diseases, hyperproliferative disorders and other diseases in which inappropriate protein kinase action is believed to play a role, such as cancer, angiogensis, atheroscelerosis, graft rejection, rheumatoid arthritis and psoriasis.

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