C₅₁H₇₅Cl₂N₃O₁₂S

Base Information

Chemical Name:C₅₁H₇₅Cl₂N₃O₁₂S
CAS No.:1616710-56-5
Molecular Formula:C₅₁H₇₅Cl₂N₃O₁₂S
Molecular Weight:1025.14
Hs Code.:

C<sub>51</sub>H<sub>75</sub>Cl<sub>2</sub>N<sub>3</sub>O<sub>12</sub>S

Synonyms:C₅₁H₇₅Cl₂N₃O₁₂S

Suppliers and Price of C₅₁H₇₅Cl₂N₃O₁₂S

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 C₅₁H₇₅Cl₂N₃O₁₂S

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₅₁H₇₅Cl₂N₃O₁₂S

There total 6 articles about C₅₁H₇₅Cl₂N₃O₁₂S 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:

: 1616710-58-7
C₅₂H₇₇Cl₂N₃O₁₂S

: 1616710-56-5
C₅₁H₇₅Cl₂N₃O₁₂S

Guidance literature:: With iodine; sodium acetate; In tetrahydrofuran; methanol; at 30 - 35 ℃; for 5h;

Reference yield:

: 10,11-didehydro-11-deoxy-6-O-methylerythromycin A,2',4-diacetate-12-(chloroacetate)

: 1616710-56-5
C₅₁H₇₅Cl₂N₃O₁₂S

Guidance literature:: Multi-step reaction with 5 steps

1: sodium iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 1 h / 20 °C

2: sodium hydride / N,N-dimethyl-formamide; mineral oil / -20 °C / Inert atmosphere

3: hydrogenchloride / acetonitrile; water / 16 h / 30 °C

4: methanol / methanol / 16 h / 30 °C

5: iodine; sodium acetate / methanol; tetrahydrofuran / 5 h / 30 - 35 °C

With hydrogenchloride; methanol; iodine; sodium acetate; sodium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium iodide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; acetonitrile; mineral oil;

Reference yield:

: 1185160-71-7
C₂₀H₂₄Cl₂N₂O₂S

: 1616710-56-5
C₅₁H₇₅Cl₂N₃O₁₂S

Guidance literature:: Multi-step reaction with 5 steps

1: sodium iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 1 h / 20 °C

2: sodium hydride / N,N-dimethyl-formamide; mineral oil / -20 °C / Inert atmosphere

3: hydrogenchloride / acetonitrile; water / 16 h / 30 °C

4: methanol / methanol / 16 h / 30 °C

5: iodine; sodium acetate / methanol; tetrahydrofuran / 5 h / 30 - 35 °C

With hydrogenchloride; methanol; iodine; sodium acetate; sodium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium iodide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; acetonitrile; mineral oil;