638207-62-2 Usage
Uses
Used in Organic Synthesis:
Methyl-2-(tert-butoxycarbonylamino)-2-cyclopropylacetate is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of new compounds with desired properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, methyl-2-(tert-butoxycarbonylamino)-2-cyclopropylacetate is used as a key intermediate in the development of new drugs and medicinal compounds. Its unique structure allows for the creation of molecules with specific pharmacological properties, potentially leading to innovative treatments for various diseases.
Used as a Building Block for Complex Molecule Synthesis:
Methyl-2-(tert-butoxycarbonylamino)-2-cyclopropylacetate also serves as a building block for the synthesis of more complex molecules. Its incorporation into larger molecular structures can enhance the pharmacological activity and selectivity of the resulting compounds, making it a valuable component in the design of advanced therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 638207-62-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,8,2,0 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 638207-62:
(8*6)+(7*3)+(6*8)+(5*2)+(4*0)+(3*7)+(2*6)+(1*2)=162
162 % 10 = 2
So 638207-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H19NO4/c1-11(2,3)16-10(14)12-8(7-5-6-7)9(13)15-4/h7-8H,5-6H2,1-4H3,(H,12,14)
638207-62-2Relevant academic research and scientific papers
Practical syntheses of both enantiomers of cyclopropylglycine and of methyl 2-cyclopropyl-2-N-Boc-iminoacetate
Larionov, Oleg V.,De Meijere, Armin
, p. 1071 - 1078 (2007/10/03)
A facile three-step synthesis of racemic cyclopropylglycine in multigram quantities from inexpensive cyclopropyl methyl ketone has been elaborated. Enzymatic hydrolysis of the N-Boc-protected methyl ester of cyclopropylglycine 9 with the inexpensive enzyme papain from Carica papaya affords both enantiomers of cyclopropylglycine (8) with enantiomeric excesses of 99% or better after deprotection under acidic conditions. Furthermore, the new cyclopropyl group-containing building block methyl 2-cyclopropyl-2-N-Boc-iminoacetate (13) was prepared by N-chlorination and subsequent dehydrochlorination with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Addition of nucleophiles to 13 offers a ready access to an unusual, orthogonally bisprotected α,α-diamino acid derivative and interesting components of rigid peptide backbones.
