cis-3a,5,6,6a-Tetrahydro-3-phenyl-4H-cyclopentisoxazole

Base Information

Chemical Name:cis-3a,5,6,6a-Tetrahydro-3-phenyl-4H-cyclopentisoxazole
CAS No.:34879-53-3
Molecular Formula:C₁₂H₁₃NO
Molecular Weight:187.241
Hs Code.:

cis-3a,5,6,6a-Tetrahydro-3-phenyl-4H-cyclopent<d>isoxazole

Synonyms:

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Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of cis-3a,5,6,6a-Tetrahydro-3-phenyl-4H-cyclopentisoxazole

Chemical Property:

Purity/Quality:

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Technology Process of cis-3a,5,6,6a-Tetrahydro-3-phenyl-4H-cyclopentisoxazole

There total 5 articles about cis-3a,5,6,6a-Tetrahydro-3-phenyl-4H-cyclopentisoxazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 69.0%

: 622-42-4
1-nitro-1-phenylmethane

: 142-29-0
cyclopentene

: 34879-53-3,34879-54-4,58074-39-8
cis-3a,5,6,6a-Tetrahydro-3-phenyl-4H-cyclopentisoxazole

Guidance literature:: With phenyl isocyanate; triethylamine; In benzene;

Reference yield: 54.0%

: 698-16-8
benzohydroximoyl chloride

: 142-29-0
cyclopentene

: 34879-53-3,34879-54-4,58074-39-8
cis-3a,5,6,6a-Tetrahydro-3-phenyl-4H-cyclopentisoxazole

Guidance literature:: In aq. phosphate buffer; acetone; at 20 ℃; pH=4;
DOI:10.1002/anie.201511730

Reference yield: 23.0%

: cyclopent-2-en-1-yl(phenyl)methanone oxime

: 62-53-3
aniline

: C₁₈H₁₈N₂O

: 34879-53-3,34879-54-4,58074-39-8
cis-3a,5,6,6a-Tetrahydro-3-phenyl-4H-cyclopentisoxazole

: 42443-82-3,65400-16-0
3-phenyl-(3ar,6ac)-4,6a-dihydro-3aH-cyclopenta[d]isoxazole

Guidance literature:: With [2,2]bipyridinyl; di-tert-butyl peroxide; copper diacetate; In acetonitrile; at 100 ℃; for 1.5h; Reagent/catalyst; Green chemistry;
DOI:10.1021/acscatal.6b02065