96014-55-0 Usage
Description
(S)-METHYL 4-(BOC-AMINO)-5-TBDMS-PENTANOATE, with the molecular formula C17H31NO4Si, is a chemical compound derived from pentanoic acid. It features a tert-butyloxycarbonyl (BOC) protecting group on the amino function and a tert-butyldimethylsilyl (TBDMS) protecting group on the hydroxyl function. (S)-METHYL 4-(BOC-AMINO)-5-TBDMS-PENTANOATE is widely utilized in organic synthesis and medicinal chemistry as a key building block for creating various pharmaceuticals and bioactive compounds. Its role as a chiral building block further enhances its value, particularly in the production of enantiomerically pure compounds for drug development and other applications.
Uses
Used in Pharmaceutical Industry:
(S)-METHYL 4-(BOC-AMINO)-5-TBDMS-PENTANOATE is used as a building block for the synthesis of various pharmaceuticals and bioactive compounds. Its presence in this industry is crucial due to its ability to contribute to the development of new drugs with enhanced efficacy and selectivity.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-METHYL 4-(BOC-AMINO)-5-TBDMS-PENTANOATE serves as an essential component for creating a range of chemical compounds. Its unique structure allows for the formation of complex molecules with specific functionalities, which can be applied in various chemical and material science applications.
Used in Medicinal Chemistry:
(S)-METHYL 4-(BOC-AMINO)-5-TBDMS-PENTANOATE is employed as a chiral building block in medicinal chemistry. Its role in the production of enantiomerically pure compounds is vital for drug development, as it helps in creating more effective and safer medications with fewer side effects.
Used in the Preparation of Peptide and Amide Derivatives:
(S)-METHYL 4-(BOC-AMINO)-5-TBDMS-PENTANOATE is also utilized in the preparation of peptide and amide derivatives, which are essential components in various biological and pharmaceutical applications. The presence of the BOC and TBDMS protecting groups allows for selective reactions and controlled synthesis of these derivatives, further expanding the compound's utility in the field.
Check Digit Verification of cas no
The CAS Registry Mumber 96014-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,0,1 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96014-55:
(7*9)+(6*6)+(5*0)+(4*1)+(3*4)+(2*5)+(1*5)=130
130 % 10 = 0
So 96014-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H35NO5Si/c1-16(2,3)23-15(20)18-13(10-11-14(19)21-7)12-22-24(8,9)17(4,5)6/h13H,10-12H2,1-9H3,(H,18,20)/t13-/m0/s1
96014-55-0Relevant articles and documents
New approach toward the total synthesis of (+)-batzellaside B
Wierzejska, Jolanta,Motogoe, Shin-Ichi,Makino, Yuto,Sengoku, Tetsuya,Takahashi, Masaki,Yoda, Hidemi
supporting information, p. 1831 - 1838,8 (2020/09/16)
A new synthetic approach to (+)-batzellaside B from naturally abundant L-pyroglutamic acid is presented in this article. The key synthetic step involves Sharpless asymmetric dihydroxylation of an olefinic substrate functionalized with an acetoxy group to
NEW ROUTES TO THE SYNTHESES OF CIS-α-(CARBOXYCYCLOPROPYL)GLYCINES FROM L-GLUTAMIC ACID. CONFORMATIONALLY RESTRICTED ANALOGUES OF THE EXCITATORY NEUROTRANSMITTER L-GLUTAMIC ACID
Shimamoto, Keiko,Ohfune, Yasufumi
, p. 3803 - 3804 (2007/10/02)
Potent neuroactive amino acids, (2S,2S,4R) and (2S,3R,4S) isomers of α-(carboxycyclopropyl)glycines (CCG-III and CCG-IV), were synthesized from L-glutamic acid via a palladium(II) catalyzed cyclopropanation of the α,β-unsaturated pyrrolidone and γ-amino-δ-lactone derivatives, respectively.
