Welcome to LookChem.com Sign In|Join Free
  • or
Ethyl (E)-4,4-difluoro-but-2-enoate is a chemical compound with the molecular formula C6H8F2O2. It is an organic ester derived from ethyl alcohol and (E)-4,4-difluorobut-2-enoic acid. ethyl (E)-4,4-difluoro-but-2-enoate is characterized by its double bond and two fluorine atoms attached to the but-2-enoate group, which gives it unique chemical properties. It is used in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and stability. The (E)-isomer indicates that the double bond has a trans configuration, which can influence its chemical behavior and potential applications.

1992-97-8

Post Buying Request

1992-97-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1992-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1992-97-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1992-97:
(6*1)+(5*9)+(4*9)+(3*2)+(2*9)+(1*7)=118
118 % 10 = 8
So 1992-97-8 is a valid CAS Registry Number.

1992-97-8Relevant academic research and scientific papers

Studies on a three-step preparation of β-fluoroalkyl acrylates from fluoroacetic esters

Jagodzinska, Monika,Huguenot, Florent,Zanda, Matteo

, p. 2042 - 2046 (2007)

β-Fluoroalkyl-acrylic esters are valuable building blocks for the synthesis of organofluorine compounds. Although the preparation of several β-fluoroalkyl-acrylates is known, a general and straightforward lab-scale methodology for the preparation of multigram amounts of these compounds from fluoroacetic esters is not available, and the related chemistry has not been investigated in detail. We now describe an optimized three-step protocol relying on: (1) Claisen-type condensation of fluoroacetic esters with ethyl acetate, using LDA as base; (2) reduction of the resulting γ-fluoro-β-keto esters by NaBH4, using toluene or benzene as solvents; (3) P2O5-promoted dehydration of the intermediate γ-fluoro-β-hydroxy esters. The methodology affords preparatively useful yields of the target compounds incorporating only fluorine atoms (CF3, CHF2, C2F5), whereas the γ-halodifluoromethyl (CClF2, CBrF2, CIF2) acrylates could not be obtained in analytically pure form from the dehydration step.

CARBOXAMIDES AS UBIQUITIN-SPECIFIC PROTEASE INHIBITORS

-

Paragraph 00301, (2019/02/25)

The present disclosure relates to modulators, such as inhibitors, of at least one pathway chosen from USP28 and USP25, pharmaceutical compositions comprising the inhibitors, and methods of using the inhibitors. The modulators, such as inhibitors, of at least one pathway chosen from USP28 and USP25 can be useful in the treatment of cancers, among other ailments.

PYRROLO AND PYRAZOLOPYRIMIDINES AS UBIQUITIN-SPECIFIC PROTEASE 7 INHIBITORS

-

Paragraph 2025; 2028, (2016/08/03)

The invention relates to inhibitors of USP7 inhibitors useful in the treatment of cancers, neurodegenerative diseases, immunological disorders, inflammatory disorders, cardiovascular diseases, ischemic diseases, viral infections and diseases, and bacterial infections and diseases, having the Formula: where m, n, X1, X2, R1-R5, R5′ and R6 are described herein.

IMPROVED PROCESS FOR PREPARING SUBSTITUTED CROTONIC ACIDS

-

Page/Page column 19; 20, (2015/12/08)

A process to prepare a compound of Formula (I) wherein R3, R4 and R5 are each selected independently from hydrogen, halogen, alkyl, alkenyl, alkynyl, alkoxyl, and wherein the alkyl, alkenyl, alkynyl, and alkoxyl may be optionally substituted with one or more halogen, alkyl, alkenyl, alkynyl, and alkoxyl.

BRUTON'S TYROSINE KINASE INHIBITORS

-

Page/Page column 166, (2014/05/24)

Disclosed herein are compounds that form covalent bonds with Bruton's tyrosine kinase (BTK). Methods for the preparation of the compounds are disclosed. Also disclosed are pharmaceutical compositions that include the compounds. Methods of using the BTK inhibitors are disclosed, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions. (Formula I)

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1992-97-8