124931-12-0 Usage
Description
DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE is an organic compound with the chemical structure featuring a phosphonate group and a carbamate moiety. It is known for its reactivity and utility in various chemical reactions and synthesis processes.
Uses
Used in Pharmaceutical Industry:
DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE is used as a reactant for the preparation of ring-expanded bryostatin analogs, which are considered as potential antitumor agents. These analogs have shown promise in the development of new cancer treatments.
Used in Chemical Synthesis:
DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE is used as a reactant in the asymmetric synthesis of pinnatoxins A and G. This process involves diastereoselective Ireland-Claisen rearrangement, ring closing metathesis, and cyclization, which are crucial steps in the synthesis of these complex molecules.
Used in Catalyst Development:
DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE is utilized in the development of Rh2(II)-catalyzed nitro-group migration reactions. The use of this phosphonate in catalysis can lead to more efficient and selective chemical transformations.
Used in Organic Chemistry:
DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE is used as a reactant in the stereoselective synthesis of cyclohexanones. The process involves phase transfer catalyzed double addition reactions, which are essential for obtaining specific stereoisomers of the target molecules.
Used in Natural Product Synthesis:
The compound is employed in the stereoselective synthesis of (+)-polyrhacitide A, a complex natural product. The synthesis involves key steps such as aldol reaction, Horner-Wardsworth-Emmons reaction, Evans acetal intramolecular oxa-Michael reaction, and diastereoselective syn reduction reaction.
Used in Material Science:
DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE is used as a reactant in the preparation of substituted furans via olefin cross-metathesis. This reaction is important for the synthesis of various furan-containing compounds, which find applications in material science and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 124931-12-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,9,3 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 124931-12:
(8*1)+(7*2)+(6*4)+(5*9)+(4*3)+(3*1)+(2*1)+(1*2)=110
110 % 10 = 0
So 124931-12-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H18NO5P/c1-5-13-15(11,14-6-2)7-8(10)9(3)12-4/h5-7H2,1-4H3
