C₄₂H₄₆O₁₄

Base Information

Chemical Name:C₄₂H₄₆O₁₄
CAS No.:848250-67-9
Molecular Formula:C₄₂H₄₆O₁₄
Molecular Weight:774.819
Hs Code.:

C<sub>42</sub>H<sub>46</sub>O<sub>14</sub>

Synonyms:C₄₂H₄₆O₁₄

Suppliers and Price of C₄₂H₄₆O₁₄

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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 C₄₂H₄₆O₁₄

Chemical Property:

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Technology Process of C₄₂H₄₆O₁₄

There total 6 articles about C₄₂H₄₆O₁₄ 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:

: 848251-54-7
C₄₈H₆₀O₁₄Si

: 848250-67-9
C₄₂H₄₆O₁₄

Guidance literature:: With pyridine; pyridine hydrogenfluoride; In acetonitrile; for 6h;
DOI:10.1021/jm049483y

Reference yield:

: 32981-86-5,172018-16-5
10-deacetylbaccatin III

: 848250-67-9
C₄₂H₄₆O₁₄

Guidance literature:: Multi-step reaction with 5 steps

1: imidazole / dimethylformamide / 25 °C

2: DMAP / CH₂Cl₂ / 25 °C

3: HF*pyridine; pyridine / acetonitrile / 0 - 25 °C

4: 85 percent / EDC; DMAP / CH₂Cl₂ / 15 h / 20 °C

5: 200 mg / HF*pyridine; pyridine / acetonitrile / 6 h

With pyridine; 1H-imidazole; dmap; pyridine hydrogenfluoride; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm049483y

Reference yield:

: 76446-91-8
13-acetyl baccatin III

: 848250-67-9
C₄₂H₄₆O₁₄

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / EDC; DMAP / CH₂Cl₂ / 15 h / 20 °C

2: 200 mg / HF*pyridine; pyridine / acetonitrile / 6 h

With pyridine; dmap; pyridine hydrogenfluoride; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; acetonitrile;
DOI:10.1021/jm049483y