20620-59-1 Usage
General Description
5-Phenyl-N-Valeric Acid Methyl Ester is a synthetic organic compound primarily used in chemical research. 5-PHENYL-N-VALERIC ACID METHYL ESTER belongs to the family of phenyl valerates and acts as a potential intermediate in the synthesis of various pharmaceutical agents. The structure of 5-Phenyl-N-Valeric Acid Methyl Ester consists of a methyl ester group attached to a valeric acid moiety, which is further connected to a phenyl ring through a nitrogen atom. The compound is generally available as a clear liquid, but its solubility, stability, and reactivity depend on the storage conditions and other specific handling instructions. No data currently exist concerning its potential toxicity, but standard protective measures should be taken while dealing with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 20620-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,2 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20620-59:
(7*2)+(6*0)+(5*6)+(4*2)+(3*0)+(2*5)+(1*9)=71
71 % 10 = 1
So 20620-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O2/c1-14-12(13)10-6-5-9-11-7-3-2-4-8-11/h2-4,7-8H,5-6,9-10H2,1H3
20620-59-1Relevant articles and documents
Mc Kelvey
, p. 187,189 (1975)
An Iron-Mesoionic Carbene Complex for Catalytic Intramolecular C-H Amination Utilizing Organic Azides
Albrecht, Martin,Keilwerth, Martin,Meyer, Karsten,Pividori, Daniel M.,Stroek, Wowa
supporting information, p. 20157 - 20165 (2021/12/09)
The synthesis of N-heterocycles is of paramount importance for the pharmaceutical industry. They are often synthesized through atom economic and environmentally unfriendly methods, generating significant waste. A less explored, but greener, alternative is
An umpolung-enabled copper-catalysed regioselective hydroamination approach to α-amino acids
Hirano, Koji,Miura, Masahiro,Nishino, Soshi
, p. 11525 - 11537 (2021/09/07)
A copper-catalysed regio- and stereoselective hydroamination of acrylates with hydrosilanes and hydroxylamines has been developed to afford the corresponding α-amino acids in good yields. The key to regioselectivity control is the use of hydroxylamine as
