122383-35-1 Usage
Uses
Used in Organic Synthesis:
(3S)-3-Isopropyl bicyclic lactam serves as a key intermediate in various organic synthesis reactions due to its reactive lactam group and unique bicyclic structure. It can be utilized to create a variety of complex organic molecules, contributing to the development of new chemical entities and materials.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, (3S)-3-isopropyl bicyclic lactam is employed as a building block for the synthesis of novel drug candidates. Its unique structure and reactivity allow for the creation of compounds with potential therapeutic properties, addressing unmet medical needs and contributing to advancements in drug discovery and development.
Used in Research and Development:
(3S)-3-Isopropyl bicyclic lactam is also used in research and development settings to explore its chemical properties and potential applications. Scientists and researchers can leverage its unique structure to investigate new reaction pathways, mechanisms, and the synthesis of innovative compounds for various purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 122383-35-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,8 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122383-35:
(8*1)+(7*2)+(6*2)+(5*3)+(4*8)+(3*3)+(2*3)+(1*5)=101
101 % 10 = 1
So 122383-35-1 is a valid CAS Registry Number.
122383-35-1Relevant articles and documents
Synthesis of heterocycles through a ruthenium-catalyzed tandem ring-closing metathesis/isomerization/N-acyliminium cyclization sequence
Ascic, Erhad,Jensen, Jakob F.,Nielsen, Thomas E.
, p. 5188 - 5191 (2011/06/26)
Tandem bicycle: In the title reaction double bonds created during ring-closing metathesis isomerize to generate reactive iminium intermediates that undergo intramolecular cyclization reactions with tethered heteroatom and carbon nucleophiles. In this way, a series of biologically interesting heterocyclic compounds can be made, including a known precursor for the total synthesis of the antiparasitic natural product harmicine. Copyright
