(2E,4E)-4-(4,4-DiMethyl-2-pentyn-1-ylidene)-2-pentenedioic Acid 1,5-DiMethyl Ester

Base Information

Chemical Name:(2E,4E)-4-(4,4-DiMethyl-2-pentyn-1-ylidene)-2-pentenedioic Acid 1,5-DiMethyl Ester
CAS No.:1176744-66-3
Molecular Formula:C₁₄H₁₈O₄
Molecular Weight:250.295
Hs Code.:
Mol file:1176744-66-3.mol

Synonyms:(2E,4E)-dimethyl 4-(4,4-dimethylpent-2-ynylidene)pent-2-enedioate

Suppliers and Price of (2E,4E)-4-(4,4-DiMethyl-2-pentyn-1-ylidene)-2-pentenedioic Acid 1,5-DiMethyl Ester

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

TRC
(2E,4E)-4-(4,4-Dimethyl-2-pentyn-1-ylidene)-2-pentenedioicAcid1,5-DimethylEster
100mg
$ 880.00

Total 5 raw suppliers

Chemical Property of (2E,4E)-4-(4,4-DiMethyl-2-pentyn-1-ylidene)-2-pentenedioic Acid 1,5-DiMethyl Ester

Chemical Property:

Boiling Point:344.2±37.0 °C(Predicted)
Density:1.056±0.06 g/cm3(Predicted)
Solubility.:DCM, Ethyl Acetate, Methanol

Purity/Quality:

>95% ^*data from raw suppliers

(2E,4E)-4-(4,4-Dimethyl-2-pentyn-1-ylidene)-2-pentenedioicAcid1,5-DimethylEster ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses (2E,4E)-4-(4,4-Dimethyl-2-pentyn-1-ylidene)-2-pentenedioic Acid 1,5-Dimethyl Ester is an intermediate in the synthesis of Terbinafine (T107500) derivatives.

Technology Process of (2E,4E)-4-(4,4-DiMethyl-2-pentyn-1-ylidene)-2-pentenedioic Acid 1,5-DiMethyl Ester

There total 1 articles about (2E,4E)-4-(4,4-DiMethyl-2-pentyn-1-ylidene)-2-pentenedioic Acid 1,5-DiMethyl Ester 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: 43.0%

: 2579-21-7
4,4-dimethylpent-2-ynal

: 5164-76-1
dimethyl glutaconate

: 1176744-66-3
(2E,4E)-dimethyl 4-(4,4-dimethylpent-2-ynylidene)pent-2-enedioate

: 1176744-68-5
C₂₀H₂₄O₄

Guidance literature:: dimethyl glutaconate; With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃;

4,4-dimethylpent-2-ynal; In tetrahydrofuran; at -78 ℃; for 1h;
DOI:10.1016/j.tet.2009.04.095