Sapintoxin d

Base Information

Chemical Name:Sapintoxin d
CAS No.:80998-07-8
Molecular Formula:C₃₀H₃₇NO₈
Molecular Weight:539.626
Hs Code.:
European Community (EC) Number:635-962-6
DSSTox Substance ID:DTXSID301001692
Nikkaji Number:J291.485I
Wikidata:Q27139925
Metabolomics Workbench ID:65958
ChEMBL ID:CHEMBL3586011
Mol file:80998-07-8.mol

Synonyms:CCRIS 7233;sapintoxin D

Suppliers and Price of Sapintoxin d

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

Usbiological
Sapintoxin D
1mg
$ 523.00

TRC
SapintoxinD
2.5mg
$ 470.00

Total 5 raw suppliers

Chemical Property of Sapintoxin d

Chemical Property:

Vapor Pressure:2.53E-20mmHg at 25°C
Boiling Point:695.8°C at 760 mmHg
Flash Point:374.6°C
PSA：142.39000
Density:1.35g/cm³
LogP:2.48030
Storage Temp.:-20°C
XLogP3:2.5
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:7
Exact Mass:539.25191714
Heavy Atom Count:39
Complexity:1140

Purity/Quality:

95% ^*data from raw suppliers

Sapintoxin D ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 22-26-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C(C2(C(C2(C)C)C3C1(C4C=C(C(=O)C4(CC(=C3)CO)O)C)O)OC(=O)C)OC(=O)C5=CC=CC=C5NC
Isomeric SMILES:C[C@@H]1[C@H]([C@@]2([C@@H](C2(C)C)[C@H]3[C@]1([C@@H]4C=C(C(=O)[C@]4(CC(=C3)CO)O)C)O)OC(=O)C)OC(=O)C5=CC=CC=C5NC
Uses Sapintoxin D is a fluorescent and highly potent phorbol ester.

Technology Process of Sapintoxin d

There total 4 articles about Sapintoxin d 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:

: 17673-25-5
phorbol

: 80998-07-8
12-O-(N-methylanthranilate) phorbol 13-acetate

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine

2: DCC / DMAP / dimethylformamide

3: 1.) 1percent HClO₄, 2.) piperidine / 1.) MeOH, 24 h, 2.) CH₂Cl₂

With piperidine; pyridine; perchloric acid; dicyclohexyl-carbodiimide; dmap; In N,N-dimethyl-formamide;
DOI:10.1016/0031-9422(88)80229-2

Reference yield:

: 41621-85-6
Phorbol 13,20-diacetate

: 80998-07-8
12-O-(N-methylanthranilate) phorbol 13-acetate

Guidance literature:: Multi-step reaction with 2 steps

1: DCC / DMAP / dimethylformamide

2: 1.) 1percent HClO₄, 2.) piperidine / 1.) MeOH, 24 h, 2.) CH₂Cl₂

With piperidine; perchloric acid; dicyclohexyl-carbodiimide; dmap; In N,N-dimethyl-formamide;
DOI:10.1016/0031-9422(88)80229-2

Reference yield:

: 120467-46-1
2-(9-fluorenylmethoxycarbonylamino)benzoic acid

: 80998-07-8
12-O-(N-methylanthranilate) phorbol 13-acetate

Guidance literature:: Multi-step reaction with 2 steps

1: DCC / DMAP / dimethylformamide

2: 1.) 1percent HClO₄, 2.) piperidine / 1.) MeOH, 24 h, 2.) CH₂Cl₂

With piperidine; perchloric acid; dicyclohexyl-carbodiimide; dmap; In N,N-dimethyl-formamide;
DOI:10.1016/0031-9422(88)80229-2