26607-48-7 Usage
Benzyl hydrogen (S)-pyrrolidine-1,2-dicarboxylate
This is a derivative of pyrrolidine, which is a heterocyclic compound with a four-membered ring containing two carbon and two nitrogen atoms.
Dicyclohexylamine
This is a type of amine, which is an organic compound containing a nitrogen atom bonded to one or more carbon atoms.
Stereochemistry
The compound has an (S)-configuration, indicating the spatial arrangement of the atoms in the molecule.
Potential applications
The compound is likely used in pharmaceutical or research applications due to its unique properties and effects.
Further research
Additional investigation and research may be necessary to fully understand the potential uses and implications of this chemical compound.
Complex structure
The compound is a complex molecule with multiple functional groups and a specific stereochemistry, which may contribute to its unique properties and potential applications.
Solubility
The solubility of the compound in various solvents may be an important factor in its potential applications and uses.
Stability
The stability of the compound under different conditions, such as temperature, pH, and exposure to light, may also be relevant to its potential uses and applications.
Reactivity
The compound may have specific reactivity with other molecules or compounds, which could be important for its potential applications in chemical reactions or synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 26607-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,0 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26607-48:
(7*2)+(6*6)+(5*6)+(4*0)+(3*7)+(2*4)+(1*8)=117
117 % 10 = 7
So 26607-48-7 is a valid CAS Registry Number.
26607-48-7Relevant articles and documents
KINETICS OF THE ALKALINE HYDROLYSIS OF SEVERAL N-BENZYLOXYCARBONYLDIPEPTIDE METHYL AND ETHYL ESTERS
Hoogwater, D. A.,Peereboom, M.
, p. 5325 - 5332 (2007/10/02)
The reaction rates of the alkaline hydrolysis of synthesized N-protected dipeptide methyl and ethyl esters were studied systematically.From the kinetic data the energies of activation, the pre-exponential factors and the reference values at 40 deg C were calculated.The rate of hydrolysis shows to be strongly dependent on the C-terminal amino acid in the sequence Gly >> Ala/Met/Phe > Leu >> Val/Pro.Surprisingly the N-terminal amino acid also exerts an effect, but in a different sequence.N-Terminal Phe in particular shows a relative accelerating effect.Remarkable is the significantly faster ester hydrolysis of glycine containing dipeptide ethyl esters in ethanol/water compared to the corresponding methyl esters in methanol/water.
