2114-14-9 Usage
Description
2-methylprop-2-enyl carbamate, also known as isobutene carbamate, is an organic compound that serves as a reagent in various chemical reactions. It is characterized by its carbamoyl group and a unique isobutene structure, which contributes to its reactivity and potential applications in different industries.
Uses
Used in Chemical Synthesis:
2-methylprop-2-enyl carbamate is used as a reagent for carbamoylation reactions, which are essential in the synthesis of various organic compounds. Its ability to selectively introduce carbamoyl groups into target molecules makes it a valuable tool in the development of new chemical entities.
Used in Stereoselective Synthesis:
In the field of organic chemistry, 2-methylprop-2-enyl carbamate is employed as a key reagent for the stereoselective synthesis of acyclic 1,3-diol systems. These systems are important structural motifs found in numerous biologically active molecules, including pharmaceuticals and natural products. The use of 2-methylprop-2-enyl carbamate in this context allows for the controlled formation of specific stereoisomers, which is crucial for the development of effective and selective drugs.
While the provided materials do not mention specific applications in different industries, the general use of 2-methylprop-2-enyl carbamate in chemical synthesis and stereoselective reactions suggests that it may find applications in the pharmaceutical, agrochemical, and materials science industries. These industries often rely on the synthesis of complex organic molecules with specific stereochemistry for the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 2114-14-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2114-14:
(6*2)+(5*1)+(4*1)+(3*4)+(2*1)+(1*4)=39
39 % 10 = 9
So 2114-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO2/c1-4(2)3-8-5(6)7/h1,3H2,2H3,(H2,6,7)
2114-14-9Relevant articles and documents
Substrate scope and stereocontrol in the Rh(II)-catalysed oxyamination of allylic carbamates
Unsworth, William P.,Lamont, Scott G.,Robertson, Jeremy
, p. 7388 - 7394 (2017/09/12)
Application of a modified Du Bois protocol for rhodium-stabilised nitrenoid generation to a variety of allylic carbamates results in 4-acetoxymethyl-1,3-oxazolidin-2-one derivatives with moderate to high levels of stereocontrol.
