39063-70-2 Usage
Heterocyclic compound
Contains a phosphorus atom The compound is a heterocyclic compound, meaning it has a ring structure with a phosphorus atom as the heteroatom.
Five-membered ring structure
1H-Phosphole based The compound has a five-membered ring structure based on 1H-phosphole, which includes the phosphorus atom as part of the ring.
Stable oxide derivative
1H-Phosphole, 2,5-dihydro-1-hydroxy-, 1-oxide The compound is a stable oxide derivative of 1H-phosphole, indicating that it has a stable structure and properties.
Use in organic chemistry
Building block for synthesis The compound is commonly used in the field of organic chemistry as a building block for the synthesis of various organic compounds.
Unique structure and reactivity
Valuable for new materials and pharmaceuticals The compound's unique structure and reactivity make it valuable for the development of new materials and pharmaceuticals.
Presence of hydroxy group
Potential candidate for biologically active molecules The presence of a hydroxy group in the molecule makes it a potential candidate for use in the design of biologically active molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 39063-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,6 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39063-70:
(7*3)+(6*9)+(5*0)+(4*6)+(3*3)+(2*7)+(1*0)=122
122 % 10 = 2
So 39063-70-2 is a valid CAS Registry Number.
39063-70-2Relevant articles and documents
A NEW REAGENT FOR THE MEDIATION OF AMIDE BOND FORMATION IN PEPTIDE SYNTHESIS.
Ramage, Robert,Ashton, Christopher P.,Hopton, David,Parrott, Maxwell J.
, p. 4825 - 4828 (2007/10/02)
The potential application of 1-oxo-1-chlorophospholane (5) as a novel reagent for the in situ activation of N α-protected amino acids for use in peptide bond forming reactions has been examined.Wherever possible, 32.4 MHz 31P nuclear magnetic resonance (n.m.r.) spectroscopy was employed to follow both the formation of the intermediate phospholanic-carboxylic mixed anhydride and the subsequent aminolysis reaction.
