32778-35-1 Usage
Uses
Used in Organic Synthesis:
3-Buten-2-one, 3-[(dimethylamino)methyl](6CI,9CI) is used as a reagent in organic synthesis for the preparation of various compounds. Its high reactivity allows for the formation of a wide range of products, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 3-Buten-2-one, 3-[(dimethylamino)methyl](6CI,9CI) is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity enable the development of new drugs with potential therapeutic applications.
Used in Other Organic Compounds Production:
3-Buten-2-one, 3-[(dimethylamino)methyl](6CI,9CI) is also utilized in the production of other organic compounds, such as dyes, pigments, and specialty chemicals. Its versatility and reactivity contribute to the development of innovative products across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 32778-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,7 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32778-35:
(7*3)+(6*2)+(5*7)+(4*7)+(3*8)+(2*3)+(1*5)=131
131 % 10 = 1
So 32778-35-1 is a valid CAS Registry Number.
32778-35-1Relevant academic research and scientific papers
HFIP Mediates a Direct C?C Coupling between Michael Acceptors and Eschenmoser's salt
Lemmerer, Miran,Riomet, Margaux,Meyrelles, Ricardo,Maryasin, Boris,González, Leticia,Maulide, Nuno
supporting information, (2022/02/10)
A direct C?C coupling process that merges Michael acceptors and Eschenmoser's salt is presented. Although reminiscent of the Morita–Baylis–Hillman reaction, this process requires no Lewis base catalyst. The underlying mechanism was unveiled by a combination of kinetic, isotopic labelling experiments as well as computational investigations, which showcased the critical role of HFIP as a superior mediator for proton-transfer events as well as the decisive role of the halide counterion.
