cerebroside C

Base Information

Chemical Name:cerebroside C
CAS No.:98677-33-9
Molecular Formula:C43H79NO9
Molecular Weight:754.102
Hs Code.:

Synonyms:

Suppliers and Price of cerebroside C

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
CerebrosideC
1mg
$ 165.00

Cayman Chemical
Cerebroside C
1mg
$ 633.00

Total 3 raw suppliers

Chemical Property of cerebroside C

Chemical Property:

Purity/Quality:

99% ^*data from raw suppliers

CerebrosideC ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses Cerebroside C is a sphingolipid that has been shown to induce cell differentiation in the fungus Schizophyllum commune. It can also induce the accumulation of antimicrobial compounds in rice leaves. Cerebroside C is found in Magnaporthe grisea.

Technology Process of cerebroside C

There total 9 articles about cerebroside C 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: 83.0%

: 175345-76-3
(2S,2'R,3R,4E,8E,3'E)-3-Acetoxy-2-(2'-acetoxy-3'-octadecenoylamino)-9-methyl-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-4,8-octadecadiene

: 70711-60-3,98677-33-9
cerebroside C

Guidance literature:: With sodium methylate; In methanol; chloroform; for 1h; Ambient temperature;

Reference yield:

: 160226-28-8
(2S,3R,4E,8E)-9-methyl-4,8-sphingadienine

: 70711-60-3,98677-33-9
cerebroside C

Guidance literature:: Multi-step reaction with 9 steps

1: PPTS / CHCl₃ / 4 h / Heating

2: 51 percent / DCC, 1-hydroxybenzotriazole / CH₂Cl₂ / 2 h / Ambient temperature

3: 65 percent / PPTS / CH₂Cl₂; methanol / 1 h / Ambient temperature

4: 93 percent / (n-Bu)4NF / tetrahydrofuran / 1 h / Ambient temperature

5: 93 percent / DMAP / CH₂Cl₂ / 2 h / Ambient temperature

6: 92 percent / pyridine / Ambient temperature

7: 73 percent / (n-Bu)4NF / tetrahydrofuran / 2 h / 0 °C

8: 54 percent / Hg(CN)2 / nitromethane; benzene / 2 h / 90 °C

9: 83 percent / NaOMe / methanol; CHCl₃ / 1 h / Ambient temperature

With pyridine; dmap; tetrabutyl ammonium fluoride; sodium methylate; mercury(II) cyanide; pyridinium p-toluenesulfonate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; nitromethane; dichloromethane; chloroform; benzene;

Reference yield:

: 175345-69-4
(2S,3R,4E,8E)-2-Amino-1,3-O-isopropylidene-9-methyl-4,8-octadecadiene

: 70711-60-3,98677-33-9
cerebroside C

Guidance literature:: Multi-step reaction with 8 steps

1: 51 percent / DCC, 1-hydroxybenzotriazole / CH₂Cl₂ / 2 h / Ambient temperature

2: 65 percent / PPTS / CH₂Cl₂; methanol / 1 h / Ambient temperature

3: 93 percent / (n-Bu)4NF / tetrahydrofuran / 1 h / Ambient temperature

4: 93 percent / DMAP / CH₂Cl₂ / 2 h / Ambient temperature

5: 92 percent / pyridine / Ambient temperature

6: 73 percent / (n-Bu)4NF / tetrahydrofuran / 2 h / 0 °C

7: 54 percent / Hg(CN)2 / nitromethane; benzene / 2 h / 90 °C

8: 83 percent / NaOMe / methanol; CHCl₃ / 1 h / Ambient temperature

With pyridine; dmap; tetrabutyl ammonium fluoride; sodium methylate; mercury(II) cyanide; pyridinium p-toluenesulfonate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; nitromethane; dichloromethane; chloroform; benzene;