477312-91-7 Usage
Uses
Used in Organic Synthesis:
[(S)-1-(phenyl 3-boronic acid)-ethyl]-carbamic acid tert-butyl ester is employed as a building block in organic synthesis, particularly for the creation of medicinally important compounds. Its unique reactivity and structural features make it a valuable component in the development of new pharmaceuticals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [(S)-1-(phenyl 3-boronic acid)-ethyl]-carbamic acid tert-butyl ester is used for the synthesis of various drugs. Its role in the development of new medications is significant, as it can contribute to the creation of more effective and targeted therapies.
Used as a Reagent in Chiral Boron Compound Preparation:
[(S)-1-(phenyl 3-boronic acid)-ethyl]-carbamic acid tert-butyl ester is also utilized as a reagent for the preparation of chiral boron compounds. These compounds are essential in asymmetric catalysis and organic electrochemistry, where they play a crucial role in enhancing the efficiency and selectivity of chemical reactions.
Used in Analytical Chemistry for Chiral Separation and Identification:
Due to its unique chirality, [(S)-1-(phenyl 3-boronic acid)-ethyl]-carbamic acid tert-butyl ester is often used as a reference compound in analytical chemistry. It aids in the chiral separation and identification of other compounds, which is vital for ensuring the purity and quality of pharmaceutical products and other chiral molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 477312-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,3,1 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 477312-91:
(8*4)+(7*7)+(6*7)+(5*3)+(4*1)+(3*2)+(2*9)+(1*1)=167
167 % 10 = 7
So 477312-91-7 is a valid CAS Registry Number.
477312-91-7Relevant academic research and scientific papers
L'Heureux, Alexandre,Martel, Alain,He, Huan,Chen, Jie,Sun, Li-Qiang,Starrett, John E.,Natale, Joanne,Dworetzky, Steven I.,Knox, Ronald J.,Harden, David G.,Weaver, David,Thompson, Mark W.,Wu, Yong-Jin
, p. 363 - 366 (2005)
The synthesis and the KCNQ2 opener activity of a novel series of acrylamides are described. Replacement of the morpholinyl moiety in (S,E)-N-[1-(3-morpholinophenyl)ethyl]-3-phenylacrylamide (1) with heteroaryl groups led to the identification of (S,E)-N-1
Arylcyclopropylcarboxylic amides as potassium channel openers
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, (2010/02/07)
The present invention provides novel arylcyclopropylcarboxylic amides and related derivatives having the general Formula I wherein R, R1, R2, R3, R4, R5, R6 and R7 are as defined
3-Heterocyclic benzylamide derivatives as potassium channel openers
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, (2010/02/07)
The present invention provides novel 3-heterocyclic benzylamides and related derivatives having the general Formula I wherein R1, R2, R3, R4, R5, R6, A and Het are as defined in the specifi
