1173664-54-4 Usage
Description
(1S,2S,3R,4S,5S)2-tert-Butoxy-carbonylamino-4,6,6-trimethylbi-cyclo[3.1.1]heptane-3-carboxylic acid is a complex bicyclic molecule with a unique stereochemical configuration of 1S,2S,3R,4S,5S. It features a tert-butoxy-carbonyl group, an amino group, and multiple methyl groups, along with a carboxylic acid group that imparts acidic properties to the compound. This intricate structure and its potentially useful properties make it a candidate for applications in organic synthesis and pharmaceutical research.
Uses
Used in Organic Synthesis:
(1S,2S,3R,4S,5S)2-tert-Butoxy-carbonylamino-4,6,6-trimethylbi-cyclo[3.1.1]heptane-3-carboxylic acid is used as a key intermediate in organic synthesis for the development of new compounds with specific functionalities. Its unique structure allows for various chemical reactions, enabling the creation of a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (1S,2S,3R,4S,5S)2-tert-Butoxy-carbonylamino-4,6,6-trimethylbi-cyclo[3.1.1]heptane-3-carboxylic acid is used as a starting material or building block for the synthesis of novel drug candidates. Its specific spatial arrangement and functional groups can be leveraged to design molecules with desired biological activities, potentially leading to the discovery of new therapeutic agents.
Used in Drug Delivery Systems:
(1S,2S,3R,4S,5S)2-tert-Butoxy-carbonylamino-4,6,6-trimethylbi-cyclo[3.1.1]heptane-3-carboxylic acid can be utilized in the development of drug delivery systems to improve the bioavailability and therapeutic efficacy of existing drugs. Its chemical properties may allow for the creation of innovative carriers or encapsulation methods, enhancing the delivery of pharmaceutical agents to target sites within the body.
Check Digit Verification of cas no
The CAS Registry Mumber 1173664-54-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,6,6 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1173664-54:
(9*1)+(8*1)+(7*7)+(6*3)+(5*6)+(4*6)+(3*4)+(2*5)+(1*4)=164
164 % 10 = 4
So 1173664-54-4 is a valid CAS Registry Number.
1173664-54-4Relevant articles and documents
Regio- and stereoselective synthesis of the enantiomers of monoterpene-based β-amino acid derivatives
Szakonyi, Zsolt,Martinek, Tamas A.,Sillanpaeae, Reijo,Fueloep, Ferenc
, p. 2442 - 2447 (2008/03/13)
The regio- and stereospecific addition of chlorosulfonyl isocyanate to cis-δ-pinene enantiomers has furnished monoterpene-fused β-lactams. The observed regioselectivity can be explained by ab initio DFT modeling of transition state structures. In contrast with the less reactive α-pinane-fused β-lactam 4, the resulting β-lactams 5 and 13 containing an amino group connected to a secondary carbon possess similar reactivity to the cycloalkane-fused analogues and can be easily converted to the β-amino acid and its protected derivatives. The base-catalyzed isomerization of the cis-amino ester afforded the corresponding trans-amino ester in moderate yield.
