332064-91-2 Usage
General Description
BOC-(R)-3-AMINO-5-HEXYNOIC ACID is a chemical compound with the molecular formula C10H17NO4. It is a derivative of 3-amino-5-hexynoic acid, with a BOC (tert-butoxycarbonyl) protecting group attached to the amino group. BOC-(R)-3-AMINO-5-HEXYNOIC ACID is a versatile building block in organic synthesis, commonly used for the preparation of peptides and peptidomimetics. Its unique structure and reactivity make it valuable for the creation of complex molecules with potential applications in drug development and materials science. BOC-(R)-3-AMINO-5-HEXYNOIC ACID is widely used in academic research and pharmaceutical industry for its capabilities in chemical modification and functionalization of molecules.
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 articles and documents
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.
