332064-91-2 Usage
Uses
Used in Academic Research:
BOC-(R)-3-AMINO-5-HEXYNOIC ACID is used as a research compound for the development of novel organic synthesis methods and the exploration of its reactivity in various chemical reactions.
Used in Pharmaceutical Industry:
BOC-(R)-3-AMINO-5-HEXYNOIC ACID is used as a key intermediate in the synthesis of bioactive peptides and peptidomimetics, contributing to the discovery of new drug candidates with potential therapeutic applications.
Used in Drug Development:
BOC-(R)-3-AMINO-5-HEXYNOIC ACID is employed as a building block in the design and synthesis of complex molecules with potential applications in drug development, facilitating the creation of innovative therapeutic agents.
Used in Materials Science:
BOC-(R)-3-AMINO-5-HEXYNOIC ACID is utilized in the development of new materials with unique properties, such as self-assembling systems and functional coatings, owing to its versatile chemical reactivity and structural features.
Check Digit Verification of cas no
The CAS Registry Mumber 332064-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,0,6 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 332064-91:
(8*3)+(7*3)+(6*2)+(5*0)+(4*6)+(3*4)+(2*9)+(1*1)=112
112 % 10 = 2
So 332064-91-2 is a valid CAS Registry Number.
332064-91-2Relevant academic research and scientific papers
Preparation method of chiral beta-(Boc-amino)-5-hexynoic acid
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, (2021/05/12)
The invention provides a preparation method of chiral beta-(Boc-amino)-5-hexynoic acid. The preparation method comprises the following steps of: (1) carrying out carboxyl activation reaction on chiral alpha-(Boc-amino)-4-pentynoic acid and chloroformate to obtain a compound as shown in a formula I; (2) carrying out substitution reaction on the compound as shown in the formula I obtained in the step (1) and diazomethane to obtain a compound as shown in a formula II; (3) carrying out Wolff rearrangement reaction on the compound as shown in the formula II obtained in the step (2) in the presence of an alkaline substance to obtain a compound as shown in a formula III; and (4) carrying out acidification reaction on the compound as shown in the formula III obtained in the step (3) to obtain a target product. The raw materials in the preparation method are easy to obtain, the reaction conditions are mild, and the preparation method is suitable for industrial large-scale production.
