C₁₁H₁₀O₅S₂

Base Information

Chemical Name:C₁₁H₁₀O₅S₂
CAS No.:1215169-40-6
Molecular Formula:C₁₁H₁₀O₅S₂
Molecular Weight:286.329
Hs Code.:

C<sub>11</sub>H<sub>10</sub>O<sub>5</sub>S<sub>2</sub>

Synonyms:

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

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Chemical Property of C₁₁H₁₀O₅S₂

Chemical Property:

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Technology Process of C₁₁H₁₀O₅S₂

There total 6 articles about C₁₁H₁₀O₅S₂ 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:

: 99-96-7
4-hydroxy-benzoic acid

: 1215169-40-6
C₁₁H₁₀O₅S₂

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / N,N-dimethyl-formamide

2: thionyl chloride

3: tin(IV) chloride

4: boron tribromide-dimethyl sulfide complex

5: sodium cyanoborohydride; chloro-trimethyl-silane

6: sodium tetrahydroborate; palladium 10% on activated carbon; potassium hydroxide / methanol / 1.33 h / Microwave irradiation

With sodium tetrahydroborate; chloro-trimethyl-silane; thionyl chloride; boron tribromide-dimethyl sulfide complex; palladium 10% on activated carbon; tin(IV) chloride; sodium cyanoborohydride; potassium carbonate; potassium hydroxide; In methanol; N,N-dimethyl-formamide; 3: |Friedel-Crafts Acylation;
DOI:10.3998/ark.5550190.0013.319

Reference yield:

: 36844-51-6
4-allyloxybenzoyl chloride

: 1215169-40-6
C₁₁H₁₀O₅S₂

Guidance literature:: Multi-step reaction with 4 steps

1: tin(IV) chloride

2: boron tribromide-dimethyl sulfide complex

3: sodium cyanoborohydride; chloro-trimethyl-silane

4: sodium tetrahydroborate; palladium 10% on activated carbon; potassium hydroxide / methanol / 1.33 h / Microwave irradiation

With sodium tetrahydroborate; chloro-trimethyl-silane; boron tribromide-dimethyl sulfide complex; palladium 10% on activated carbon; tin(IV) chloride; sodium cyanoborohydride; potassium hydroxide; In methanol; 1: |Friedel-Crafts Acylation;
DOI:10.3998/ark.5550190.0013.319

Reference yield:

: 1215169-50-8
(4-allyloxyphenyl)-(3-hydroxythiophen-2-yl)-methanone

: 1215169-40-6
C₁₁H₁₀O₅S₂

Guidance literature:: Multi-step reaction with 2 steps

1: sodium cyanoborohydride; chloro-trimethyl-silane

2: sodium tetrahydroborate; palladium 10% on activated carbon; potassium hydroxide / methanol / 1.33 h / Microwave irradiation

With sodium tetrahydroborate; chloro-trimethyl-silane; palladium 10% on activated carbon; sodium cyanoborohydride; potassium hydroxide; In methanol;
DOI:10.3998/ark.5550190.0013.319