1219015-26-5 Usage
General Description
(R)-2-((tert-butoxycarbonyl)amino)oct-7-enoic acid is a compound known for its potential use in drug development, particularly as a building block in the synthesis of pharmaceuticals. It is an amino acid derivative with a tert-butoxycarbonyl (Boc) protecting group and a double bond at the 7th carbon position. The Boc protecting group can be removed under mild conditions, making it a useful intermediate for the synthesis of peptides and other complex molecules. Its unique structure and functional groups make it a valuable tool in organic chemistry and medicinal chemistry research. Additionally, it has been studied for its potential biological activities, although more research is needed to fully understand its pharmacological properties. Overall, (R)-2-((tert-butoxycarbonyl)amino)oct-7-enoic acid shows promise as a versatile and valuable compound in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1219015-26-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,0,1 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1219015-26:
(9*1)+(8*2)+(7*1)+(6*9)+(5*0)+(4*1)+(3*5)+(2*2)+(1*6)=115
115 % 10 = 5
So 1219015-26-5 is a valid CAS Registry Number.
1219015-26-5Relevant articles and documents
Asymmetric Synthesis of Protected Unnatural α-Amino Acids via Enantioconvergent Nickel-Catalyzed Cross-Coupling
Freas, Dylan J.,Fu, Gregory C.,Yang, Ze-Peng
, p. 8614 - 8618 (2021/06/28)
Interest in unnatural α-Amino acids has increased rapidly in recent years in areas ranging from protein design to medicinal chemistry to materials science. Consequently, the development of efficient, versatile, and straightforward methods for their enanti
