Cholesteryl 9-anthracenecarboxylate

Base Information

• Chemical Name: Cholesteryl 9-anthracenecarboxylate
• CAS No.: 2641-40-9
• Molecular Formula: C₄₂H₅₄O₂
• Molecular Weight: 590.89
• DSSTox Substance ID: DTXSID20437793
• Nikkaji Number: J1.085.475J
• Wikidata: Q82253355
• Mol file: 2641-40-9.mol

Synonyms:Cholesteryl 9-anthracenecarboxylate;2641-40-9;9-Anthracenecarboxylic acid cholesteryl ester;[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] anthracene-9-carboxylate;CHOLESTERYL9-ANTHRACENECARBOXYLATE;SCHEMBL592392;DTXSID20437793;Cholesteryl 9-anthracene carboxylate;MFCD00674495;AKOS032953563;Anthracene-9-carboxylic acid 3beta-cholesteryl ester;(3beta)-Cholest-5-en-3-yl anthracene-9-carboxylate

Chemical Property of Cholesteryl 9-anthracenecarboxylate

Chemical Property:

• Melting Point: 196-197 °C(lit.)
• Boiling Point: 685.0±34.0 °C(Predicted)
• PSA: 26.30000
• Density: 1.10±0.1 g/cm3(Predicted)
• LogP: 11.55980
• Storage Temp.: −20°C
• Solubility.: DMF: soluble
• XLogP3: 13.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 8
• Exact Mass: 590.412380961
• Heavy Atom Count: 44
• Complexity: 1040

Purity/Quality:

98% ^*data from raw suppliers

Cholesteryl 9-anthracenecarboxylate ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C5=C6C=CC=CC6=CC7=CC=CC=C75)C)C
• Isomeric SMILES: C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)OC(=O)C5=C6C=CC=CC6=CC7=CC=CC=C75)C)C

Technology Process of Cholesteryl 9-anthracenecarboxylate

There total 3 articles about Cholesteryl 9-anthracenecarboxylate 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:

→ H2N-glycyl-prolyl-glutamyl-glycyl-isoleucyl-tryptophanyl-glycyl-glutamyl-glycine(Gly-Pro-Gln-Gly-ne-Tip-Gly-Gln-Gly)-amidopolybenzyl-L-aspartate + cholesteryl anthracene-9-carboxylate (2641-40-9)

Guidance literature:

Reference yield:

→ Cholesterin- (2641-40-9)

Guidance literature:

Cholesterin, Anthracen-9-carbonsaeurechlorid, Py. (Siedetemp.);

DOI:10.1021/ja01083a011

Reference yield:

→ 9-Anthracencarbonsaeure-cholesterylester (2641-40-9)

Guidance literature:

Anthracen-9-carbonsaeurechlorid, Cholesterol;

DOI:10.1073/pnas.67.2.579

Refernces

• 1、 -. "CONJUGATE FOR RETENTION IN BLOOD AND CANCER TISSUE-SPECIFIC DRUG DELIVERY". . . Retrieved 2008/06/13.