Keracyanin

Base Information

• Chemical Name: Keracyanin
• CAS No.: 18719-76-1
• Deprecated CAS: 1329-47-1,16067-08-6,27661-63-8,28603-07-8,29894-06-2,31921-38-7,31939-23-8,52918-66-8,64577-68-0,65941-77-7,141914-92-3
• Molecular Formula: C27H31 O15 . Cl
• Molecular Weight: 630.987
• European Community (EC) Number: 242-528-6
• UNII: V0N2VMB4FV
• DSSTox Substance ID: DTXSID00927864
• Wikipedia: Antirrhinin
• Wikidata: Q3814728
• NCI Thesaurus Code: C81330
• Metabolomics Workbench ID: 143195
• ChEMBL ID: CHEMBL592218
• Mol file: 18719-76-1.mol

Synonyms:cyanidin chloride 3-rhamnoglucoside;cyaninoside chloride;keracyanin;Meralop;meralops

Chemical Property of Keracyanin

Chemical Property:

• Melting Point: 175℃
• PSA: 252.36000
• LogP: -3.76220
• Storage Temp.: −20°C
• Solubility.: Methanol (Slightly), Water (Slightly)
• Hydrogen Bond Donor Count: 10
• Hydrogen Bond Acceptor Count: 15
• Rotatable Bond Count: 6
• Exact Mass: 630.1351480
• Heavy Atom Count: 43
• Complexity: 883

Purity/Quality:

98% ^*data from raw suppliers

Cyanidin-3-O-rutinoside chloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O.[Cl-]
• Isomeric SMILES: C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O.[Cl-]
• Uses: Cyanidin 3-O-Rutinoside retards absorption of carbohydrates by inhibition of α-glucosidase which may be useful as a potential inhibitor for prevention and treatment of diabetes mellitus.

Technology Process of Keracyanin

There total 2 articles about Keracyanin 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: 60.0%

rutin (153-18-4) → antirrhinin (18719-76-1)

Guidance literature:

With hydrogenchloride; amalgamated zinc; In methanol; for 0.166667h;

DOI:10.1016/0040-4039(95)00809-Q

Reference yield:

→ antirrhinin (18719-76-1)

Guidance literature:

With tetrahydrofuran; lithium aluminium tetrahydride; anschliessend Behandeln mit wss. Salzsaeure;

Reference yield:

antirrhinin (18719-76-1) + 2-oxo-propionic acid (127-17-3) → 10-carboxy-pyranocyanidin-3-O-rutinoside

Guidance literature:

In water; at 35 ℃; for 120h; pH=2.6;

DOI:10.1021/jf061085b

upstream raw materials:

rutin

Refernces