20059-62-5 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 2-methyl-N-phenylalaninate is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
methyl 2-methyl-N-phenylalaninate is utilized as a key component in the production of agrochemicals, helping to create effective solutions for agricultural applications.
Used in Organic Synthesis:
Methyl 2-methyl-N-phenylalaninate is employed as a versatile building block in organic synthesis, enabling the creation of a wide range of chemical compounds for various industries.
Used in Asymmetric Catalysis:
methyl 2-methyl-N-phenylalaninate serves as a chiral ligand in asymmetric catalysis, playing a crucial role in the development of enantioselective reactions and the production of enantiomerically pure compounds.
Used in Peptide Synthesis:
Methyl 2-methyl-N-phenylalaninate is used as an intermediate in the synthesis of peptides, contributing to the development of bioactive peptides for research and therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 20059-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,5 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20059-62:
(7*2)+(6*0)+(5*0)+(4*5)+(3*9)+(2*6)+(1*2)=75
75 % 10 = 5
So 20059-62-5 is a valid CAS Registry Number.
20059-62-5Relevant academic research and scientific papers
Chemistry of Tertiary Carbon Center in the Formation of Congested C?O Ether Bonds
Hirata, Goki,Takeuchi, Kentarou,Shimoharai, Yusuke,Sumimoto, Michinori,Kaizawa, Hazuki,Nokami, Toshiki,Koike, Takashi,Abe, Manabu,Shirakawa, Eiji,Nishikata, Takashi
supporting information, p. 4329 - 4334 (2020/12/23)
Nucleophilic substitutions, including SN1 and SN2, are classical and reliable reactions, but a serious drawback is their intolerance for both bulky nucleophiles and chiral tertiary alkyl electrophiles for the synthesis of a chiral quaternary carbon center. An SRN1 reaction via a radical species is another conventional method used to carry out substitution reactions of bulky nucleophiles and alkyl halides, but chiral tertiary alkyl electrophiles cannot be used. Therefore, a stereospecific nucleophilic substitution reaction using chiral tertiary alkyl electrophiles and bulky nucleophiles has not yet been well studied. In this paper, we describe the reaction of tertiary alkyl alcohols and non-chiral or chiral α-bromocarboxamides as a tertiary alkyl source for the formation of congested ether compounds possessing two different tertiary alkyl groups on the oxygen atom with stereoretention.
