638207-62-2 Usage
General Description
Methyl-2-(tert-butoxycarbonylamino)-2-cyclopropylacetate is a chemical compound that belongs to the ester class of compounds. It is characterized by a methyl group, a cyclopropyl group, and a tert-butoxycarbonylamino group attached to a central acetate group. This chemical is commonly used as a reagent in organic synthesis and pharmaceutical research. It has potential applications in the development of new drugs and medicinal compounds due to its unique structure and reactivity. Additionally, it can serve as a building block for the synthesis of more complex molecules with specific pharmacological properties. Overall, methyl-2-(tert-butoxycarbonylamino)-2-cyclopropylacetate is a versatile compound with diverse potential applications in the fields of chemistry and medicine.
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 articles and documents
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.
