C₁₅H₁₈O₂

Base Information

Chemical Name:C₁₅H₁₈O₂
CAS No.:1352740-84-1
Molecular Formula:C₁₅H₁₈O₂
Molecular Weight:230.307
Hs Code.:

C<sub>15</sub>H<sub>18</sub>O<sub>2</sub>

Synonyms:

Suppliers and Price of C₁₅H₁₈O₂

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₁₅H₁₈O₂

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₅H₁₈O₂

There total 4 articles about C₁₅H₁₈O₂ 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:

: 1352740-82-9
(E)-benzyl 8-iodooct-2-enoate

: benzyl 2-cyclohexylideneacetate

: 1352740-84-1
C₁₅H₁₈O₂

Guidance literature:: With triphenylstannylcobaloxime; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 50 ℃; for 16h; Inert atmosphere; Sanlamp irradiation;
DOI:10.1002/anie.201105235

Reference yield:

: 1352741-10-6
C₁₅H₁₉BrO₂

: benzyl 2-cyclohexylideneacetate

: 1352740-84-1
C₁₅H₁₈O₂

Guidance literature:: Multi-step reaction with 2 steps

1: sodium iodide / acetone / 1.5 h / 0 - 56 °C

2: triphenylstannylcobaloxime; N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / 50 °C / Inert atmosphere; Sanlamp irradiation

With triphenylstannylcobaloxime; N-ethyl-N,N-diisopropylamine; sodium iodide; In acetone; acetonitrile; 2: Heck-type coupling;
DOI:10.1002/anie.201105235

Reference yield:

: 57978-00-4
6-bromohexanal

: benzyl 2-cyclohexylideneacetate

: 1352740-84-1
C₁₅H₁₈O₂

Guidance literature:: Multi-step reaction with 3 steps

1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium bromide / acetonitrile / 0.5 h / 0 °C / Inert atmosphere

1.2: 1 h / Inert atmosphere

2.1: sodium iodide / acetone / 1.5 h / 0 - 56 °C

3.1: triphenylstannylcobaloxime; N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / 50 °C / Inert atmosphere; Sanlamp irradiation

With triphenylstannylcobaloxime; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; sodium iodide; lithium bromide; In acetone; acetonitrile; 3.1: Heck-type coupling;
DOI:10.1002/anie.201105235