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Cyclobutanol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 2919-23-5. Pack Sizes: 10 g; 25 g. Product ID: HY-W013042.
Intermediate in the preparation of carbocyclic nucleoside derivatives. Group: Biochemicals. Alternative Names: [1S-(1α,2 β,3 β)]-3-Hydroxy-1,2-cyclobutanedimethanol 1,2-Dibenzoate. Grades: Highly Purified. CAS No. 132294-17-8. Pack Sizes: 5mg. US Biological Life Sciences.
Cis-3-methoxycyclobutan-1-ol, a synthetic organic compound utilized as a reagent in chemical synthesis, has exhibited promise as a pivotal intermediate in producing numerous bioactive molecules including anti-inflammatory, anti-tumor, and analgesic agents. Synonyms: cis-3-Methoxycyclobutanol; Cyclobutanol, 3-methoxy-, cis-. CAS No. 1807941-46-3. Molecular formula: C5H10O2. Mole weight: 102.13.
Tris (dibenzylideneacetone)dipalladium (0) chloroform adduct
Tris (dibenzylideneacetone)dipalladium (0) chloroform adduct. Uses: Used for pd-catalyzed asymmetric arylation, vinylation, and allenylation of tert-cyclobutanols via enantioselective c-c bond cleavage. used for synthesis of chiral chromans through the pd-catalyzed asymmetric allylic alkylation (aaa). catalyst for double n-arylation of primary amines to synthesize multisubstituted carbazoles from 2,2'biphenylylene ditriflates. paladium catalyst for regioand enanti. Group: Salt. Alternative Names: Tris(dibenylideneacetone)dipalladium-chloroform; tris- (dibenzylideneacetone)-dipalladium (o)-chloroform adduct; tris (dibenzylideneacetone)-dipalladium (0) chloroform adduct; DIPALLADIUM (0)TRIS (DIBENZYLIDENEACETONE)-CHLOROFORM ADDUCT; tris(dibenzylideneacetone) dipalladium(0)chloroform adduct; GC10022; I14-10041; tris(dibenzylideneacetone) dipalladium chloroform; tris (dibenzylideneacetone)dipa. CAS No. 52522-40-4. Product ID: chloroform; (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium. Molecular formula: 1035.103g/mol. Mole weight: C52H43Cl3O3Pd2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C(Cl)(Cl)Cl. [Pd]. [Pd]. InChI=1S/3C17H14O. CHCl3. 2Pd/c3*18-17 (13-11-15-7-3-1-4-8-15) 14-12-16-9-5-2-6-10-16; 2-1 (3) 4; ; /h3*1-14H; 1H; ; /b3*13-11+, 14-12+; ; ;. LNAMMBFJMYMQTO-FNEBRGMMSA-N.
Tris (dibenzylideneacetone)dipalladium (0) chloroform adduct
Used for Pd-catalyzed asymmetric arylation, vinylation, and Allenylation of tert-cyclobutanols via enantioselective C-C Bond cleavage. Used for synthesis of chiral chromans through the Pd-catalyzed asymmetric allylic alkylation (AAA). Catalyst for double N-arylation of primary amines to synthesize multisubstituted carbazoles from 2,2'biphenylylene ditriflates. Paladium catalyst for regioand enantioselective allylic alkylation of ketones through allyl enol carbonates. Used for Pd-catalyzed enantioselective C-3 allylation of 3-substituted-1H-indoles using trialkylboranes. Used for enantioselective construction of spirocyclic oxindolic cyclopentanes by Pd-catalyzed trimethylenemethane- [3+2]-cycloaddition. Used for Pd-catalyzed insertion of α-diazoesters into vinyl halides to generate α,β-unsaturated γ-amino Esters. Pd catalyst for decarboxylative asymmetric allylic alkylation of enol carbonates. Palladium catalyst for asymmetric addition of oxindoles and allenes. Catalyst for diastereoand enantioselective formal [3+2]-cycloaddition between substituted vinylcyclopropanes and electron-deficient olefins. Used for Pd-catalyzed asymmetric decarboxylative cycloaddition of vinylethylene carbonates with Michael sacceptors. Catalyst for enantioselective [6+4] cycloaddition of vinyl oxetanes with azadienes to access ten-membered heterocycles. Group: Palladium series
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