C₄₅H₅₉NO₁₈

Base Information

Chemical Name:C₄₅H₅₉NO₁₈
CAS No.:675584-89-1
Molecular Formula:C₄₅H₅₉NO₁₈
Molecular Weight:901.959
Hs Code.:

C<sub>45</sub>H<sub>59</sub>NO<sub>18</sub>

Synonyms:C₄₅H₅₉NO₁₈

Suppliers and Price of C₄₅H₅₉NO₁₈

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 C₄₅H₅₉NO₁₈

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₅H₅₉NO₁₈

There total 5 articles about C₄₅H₅₉NO₁₈ 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:

: 675584-87-9
C₆₀H₈₁NO₂₀Si

: 675584-89-1
C₄₅H₅₉NO₁₈

Guidance literature:: C₆₀H₈₁NO₂₀Si; With pyridine; hydrogen fluoride; In acetonitrile; at 20 ℃; for 2h;

With methanol; acetyl chloride; In dichloromethane; at 20 ℃;
DOI:10.1016/j.bmcl.2005.08.066

Reference yield:

: 675584-85-7
C₃₉H₅₀O₁₄Si

: 675584-89-1
C₄₅H₅₉NO₁₈

Guidance literature:: Multi-step reaction with 3 steps

1.1: 76 percent / Et₄N(BH₄) / methanol / 2.5 h / -40 - 0 °C

2.1: DMAP; EDCI / CH₂Cl₂ / 1.5 h / 20 °C

3.1: HF; pyridine / acetonitrile / 2 h / 20 °C

3.2: 248 mg / AcCl; MeOH / CH₂Cl₂ / 20 °C

With pyridine; dmap; hydrogen fluoride; tetraethylammonium borohydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2005.08.066

Reference yield:

: 675584-84-6
C₃₈H₅₂O₁₃Si

: 675584-89-1
C₄₅H₅₉NO₁₈

Guidance literature:: Multi-step reaction with 4 steps

1.1: 230 mg / imidazole / CH₂Cl₂ / 1.5 h / 40 °C

2.1: 76 percent / Et₄N(BH₄) / methanol / 2.5 h / -40 - 0 °C

3.1: DMAP; EDCI / CH₂Cl₂ / 1.5 h / 20 °C

4.1: HF; pyridine / acetonitrile / 2 h / 20 °C

4.2: 248 mg / AcCl; MeOH / CH₂Cl₂ / 20 °C

With pyridine; 1H-imidazole; dmap; hydrogen fluoride; tetraethylammonium borohydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2005.08.066