63891-88-3 Usage
Description
Ethyl 4-broMo-2,2-diMethylacetoacetate, also known as Ethyl 4-Bromo-2,2-Dimethyl-3-Oxobutanoate, is a chemical compound with a unique molecular structure that features a bromo group and a methyl group attached to a central acetoacetate core. Ethyl 4-broMo-2,2-diMethylacetoacetate has been identified for its potential applications in various fields due to its specific chemical properties.
Uses
Used in Pharmaceutical Industry:
Ethyl 4-broMo-2,2-diMethylacetoacetate is used as an IRAK4 inhibitor for treating a wide range of diseases, including inflammatory, autoimmune, cardiovascular, central nervous system, dermatology, bone, and ophthalmic conditions. Its application as an IRAK4 inhibitor helps in modulating the immune response and reducing inflammation, making it a promising candidate for therapeutic intervention in these diseases.
Additionally, Ethyl 4-broMo-2,2-diMethylacetoacetate has been found to be effective in cancer treatment. As an IRAK4 inhibitor, it can potentially disrupt the signaling pathways involved in cancer cell growth and proliferation, offering a new avenue for cancer therapy.
Check Digit Verification of cas no
The CAS Registry Mumber 63891-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,9 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63891-88:
(7*6)+(6*3)+(5*8)+(4*9)+(3*1)+(2*8)+(1*8)=163
163 % 10 = 3
So 63891-88-3 is a valid CAS Registry Number.
63891-88-3Relevant articles and documents
Synthesis and biological evaluation of simplified mycothiazole analogues
Mahler, Graciela,Serra, Gloria,Dematteis, Sylvia,Saldana, Jenny,Dominguez, Laura,Manta, Eduardo
, p. 1309 - 1311 (2006)
Thiazoline and oxazoline analogues of the natural product mycothiazole were synthesized from a common intermediate and evaluated in vitro against HCT-15 colon cancer cells and L4 larvae of nematode Nippostrongylus brasiliensis. The nature of the heterocyclic moiety seems to modulate the cytotoxic or anthelmintic activity.
Synthesis of enantiomerically enriched α,α-disubstituted β,γ-epoxy esters using hydrolytic kinetic resolution catalyzed by salenCo(III)
Viera, Ignacio,Manta, Eduardo,Gonzalez, Lucia,Mahler, Graciela
experimental part, p. 631 - 635 (2010/08/03)
Novel α,α-disubstituted epoxy esters were prepared in enantiopure form by hydrolytic kinetic resolution (HKR) of the corresponding racemic mixtures using chiral salenCo(III) as catalyst. The methodology provides a convenient route to enantioenriched β,γ-epoxy esters 2a, 2c and 2d.
Method for Synthesis of 2,5-Dioxane-1,4-Diones
-
Page/Page column 3, (2008/06/13)
The invention relates to a novel method for the synthesis of 2,5-dioxane-1,4-diones having formula (I), comprising the oxidation of the ketone function of a cyclic compound having formula (II), wherein R1, R2, R3 and R4 independently represent the hydrogen atom, halo, (C2-C6) alkenyl, (C3-C7)cycloalkyl, cyclohexenyl and a radical having formula —(CH2)m—V—W.