137452-35-8

Basic information

• Product Name: tert-butyl (S)-2-(benzyloxycarbonylamino)-5-iodopentanoate
• Synonyms: tert-butyl (S)-2-(benzyloxycarbonylamino)-5-iodopentanoate
• CAS NO: 137452-35-8
• Molecular Weight: 433.286
• Mol File: 137452-35-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: tert-butyl (S)-2-(benzyloxycarbonylamino)-5-iodopentanoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (S)-2-(benzyloxycarbonylamino)-5-iodopentanoate(137452-35-8)
• EPA Substance Registry System: tert-butyl (S)-2-(benzyloxycarbonylamino)-5-iodopentanoate(137452-35-8)

Safety Data

• Hazardous Substances Data: 137452-35-8(Hazardous Substances Data)

Upstream product

• 81470-51-1 tert-butyl N-benzyloxycarbonyl-L-pyroglutamate 
• 35418-16-7 L-t-butyl pyroglutamate 
• 540-88-5 acetic acid tert-butyl ester 
• 124620-51-5 (S)-tert-butyl 2-(((benzyloxy)carbonyl)amino)-5-hydroxypentanoate 

Downstream Products

• 1108725-36-5 tert-butyl (S)-5-azido-2-(benzyloxycarbonylamino)pentanoate 

Relevant articles and documents

Stereoselective construction of the 5-hydroxy diazabicyclo[4.3.1]decane-2-one scaffold, a privileged motif for FK506-binding proteins

A stereoselective synthesis of a derivatized bicyclic [4.3.1]decane scaffold based on an acyclic precursor is described. The key steps involve a Pd-catalyzed sp3-sp2 Negishi-coupling, an asymmetric Shi epoxidation, and an intramolecular epoxide opening. Representative derivatives of this novel scaffold were synthesized and found to be potent inhibitors of the psychiatric risk factor FKBP51, which bound to FKBP51 with the intended molecular binding mode. (Chemical Equation Presented).

DIAZABICYCLO[4.3.1]DECANE DERIVATIVES FOR TREATMENT OF PSYCHIATRIC DISORDERS

The present invention relates to diazabicyclo[4.3.1 ]decane derivatives (I), pharmaceutically acceptable salts of these compounds and pharmaceutical compositions containing at least one of these compounds together with pharmaceutically acceptable carrier, excipient and/or diluents. Said diazabicyclo[4.3.1]decane derivatives are specific inhibitors of the FK506 binding proteins (FKBP's) and can be used for prophylaxis and/or treatment of psychiatric disorders and neurodegenerative diseases, disorders and conditions.

Synthesis of unnatural homologues of deoxypyridinoline as possible internal standards in analytical detection of pyridinolinic cross-links of collagen

Three homologues of the collagen cross-links deoxypyridinoline, differing in the length of the side chain at the aromatic nitrogen, have been efficiently synthesized as possible internal standards in the quantitative analyses of pyridinolines. The first has a one-carbon shorter N-chain, while other two have a one-carbon and a two-carbon longer N-chain. The stereogenic centers are introduced stereoselectively using Williams' glycine template methodology and oxazinones to generate chirality and to suitably protect the amino acid functionality during assembly of the pyridinoline nucleus.