C₄₇H₄₈Cl₃NO₁₃

Base Information

Chemical Name:C₄₇H₄₈Cl₃NO₁₃
CAS No.:221366-41-2
Molecular Formula:C₄₇H₄₈Cl₃NO₁₃
Molecular Weight:941.256
Hs Code.:

C<sub>47</sub>H<sub>48</sub>Cl<sub>3</sub>NO<sub>13</sub>

Synonyms:

Suppliers and Price of C₄₇H₄₈Cl₃NO₁₃

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 C₄₇H₄₈Cl₃NO₁₃

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₇H₄₈Cl₃NO₁₃

There total 11 articles about C₄₇H₄₈Cl₃NO₁₃ 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:

: 98-88-4
benzoyl chloride

: 221366-41-2
C₄₇H₄₈Cl₃NO₁₃

Guidance literature:: Multi-step reaction with 4 steps

1: 3(CH₂)3>4N(HSO₄), NaOH / CH₂Cl₂

2: 73.7 percent / N-iodosuccinimide, triflic acid / CH₂Cl₂

3: 62 percent / trichloroacetic acid / CH₂Cl₂

4: DBU / CH₂Cl₂

With sodium hydroxide; N-iodo-succinimide; trifluorormethanesulfonic acid; tetrabutylammonium perchlorate; 1,8-diazabicyclo[5.4.0]undec-7-ene; trichloroacetic acid; In dichloromethane;
DOI:10.1016/S0957-4166(98)00494-7

Reference yield:

: 162466-36-6
(3aR,4S,6S,7S,7aR)-4-Ethylsulfanyl-2-methoxy-2,6-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-ol

: 221366-41-2
C₄₇H₄₈Cl₃NO₁₃

Guidance literature:: Multi-step reaction with 6 steps

1: NaH / dimethylformamide

2: aq. AcOH

3: pyridine

4: 73.7 percent / N-iodosuccinimide, triflic acid / CH₂Cl₂

5: 62 percent / trichloroacetic acid / CH₂Cl₂

6: DBU / CH₂Cl₂

With pyridine; N-iodo-succinimide; trifluorormethanesulfonic acid; sodium hydride; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; trichloroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0957-4166(98)00494-7

Reference yield:

: 36793-04-1
tert-Butyl β-D-galactopyranoside

: 221366-41-2
C₄₇H₄₈Cl₃NO₁₃

Guidance literature:: Multi-step reaction with 7 steps

1: 45 percent / p-TsOH / dimethylformamide / 80 °C

2: NaH / dimethylformamide

3: HCl, MeOH / CH₂Cl₂

4: 3(CH₂)3>4N(HSO₄), NaOH / CH₂Cl₂

5: 73.7 percent / N-iodosuccinimide, triflic acid / CH₂Cl₂

6: 62 percent / trichloroacetic acid / CH₂Cl₂

7: DBU / CH₂Cl₂

With hydrogenchloride; methanol; sodium hydroxide; N-iodo-succinimide; trifluorormethanesulfonic acid; tetrabutylammonium perchlorate; sodium hydride; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; trichloroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0957-4166(98)00494-7