Cas no 88515-58-6 (Rosamultin)

Rosamultin structure
Rosamultin structure
Product Name:Rosamultin
CAS No:88515-58-6
MF:C36H58O10
MW:650.839732646942
CID:724344
PubChem ID:21122581
Update Time:2024-10-26

Rosamultin Chemical and Physical Properties

Names and Identifiers

    • Urs-12-en-28-oic acid,2,3,19-trihydroxy-, b-D-glucopyranosyl ester, (2a,3b)-
    • Rosamultin
    • Rosamutin
    • Tormentic acid glucosyl
    • ursolazuroside 1
    • (+)-Rosamultin
    • 28-Glucosyltormentate
    • 2alpha,3beta,19alpha-Trihydroxylurs-12-en-28-oic acid-28-O-beta-D-glucopyranoside
    • Glucosyl tormentate
    • Kajichgoside f1
    • Tormentic acid 28-O-glucosyl ester
    • [(2R,3S,4R,5R,6S)-3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2S,4aR,6aR,6bS,10S,11S,12aS)-1,10
    • 2α,3β,19α-Trihydroxylurs-12-en-28-oic acid-28-O-β-D-glucopyranoside
    • CHEMBL501885
    • EX-A8013Q
    • CS-0022897
    • HY-N2565
    • 88515-58-6
    • AKOS037515228
    • AC-35015
    • MS-30963
    • .beta.-D-Glucopyranose, 1-O-[(2.alpha.,3.beta.)-2,3,19-trihydroxy-28-oxours-12-en-28-yl]-
    • [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate
    • s3287
    • [(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate
    • D-glucopyranose, 1-O-[(2alpha,3beta)-2,3,19-trihydroxy-28-oxours-12-en-28-yl]-
    • Urs-12-en-28-oic acid, 2,3,19-trihydroxy-, beta-D-glucopyranosyl ester, (2alpha,3beta)-
    • FT-0775928
    • FT-0775889
    • DA-57519
    • (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1R,2R,4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylate
    • Inchi： 1S/C36H58O10/c1-18-10-13-36(30(43)46-29-26(41)25(40)24(39)21(17-37)45-29)15-14-33(5)19(27(36)35(18,7)44)8-9-23-32(4)16-20(38)28(42)31(2,3)22(32)11-12-34(23,33)6/h8,18,20-29,37-42,44H,9-17H2,1-7H3/t18-,20-,21-,22+,23-,24-,25+,26-,27-,28+,29+,32+,33-,34-,35-,36+/m1/s1
    • InChI Key： MLKQAGPAYHTNQQ-BRDPIYJESA-N
    • SMILES： C([C@]12CC[C@@H](C)[C@](O)(C)[C@H]1C1=CC[C@@H]3[C@]4(C[C@@H](O)[C@H](O)C(C)(C)[C@@H]4CC[C@@]3(C)[C@@]1(CC2)C)C)(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1

Computed Properties

  • Exact Mass: 650.40300
  • Monoisotopic Mass: 650.40299804 g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 7
  • Hydrogen Bond Acceptor Count: 10
  • Heavy Atom Count: 46
  • Rotatable Bond Count: 4
  • Complexity: 1250
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 15
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 177
  • Molecular Weight: 650.8
  • XLogP3: 3.2

Experimental Properties

  • Color/Form: Powder
  • Density: 1.31±0.1 g/cm3 (20 oC 760 Torr),
  • Melting Point: 218-220 oC (chloroform methanol )
  • Boiling Point: 741.5±0.0 °C at 760 mmHg
  • Flash Point: 223.6±0.0 °C
  • Solubility: Insuluble (6.51E-4 g/L) (25 oC),
  • PSA: 177.14000
  • LogP: 2.43370
  • Vapor Pressure: 0.0±0.0 mmHg at 25°C

Rosamultin Security Information

Rosamultin Pricemore >>

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Rosamultin Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Sodium methoxide Solvents: Methanol ;  1 h, rt
Reference
Hepatoprotective triterpenes from traditional Tibetan medicine Potentilla anserina
Morikawa, Toshio; et al, Phytochemistry (Elsevier), 2014, 102, 169-181

Production Method 2

Reaction Conditions
1.1 Reagents: Sodium borohydride Solvents: Methanol ;  1 h, 0 °C
1.2 Reagents: Acetone ;  0 °C
Reference
Hepatoprotective triterpenes from traditional Tibetan medicine Potentilla anserina
Morikawa, Toshio; Ninomiya, Kiyofumi; Imura, Katsuya; Yamaguchi, Takahiro; Akagi, Yoshinori; et al, Phytochemistry (Elsevier), 2014, 102, 169-181

Production Method 3

Reaction Conditions
1.1 4 d
Reference
Biotransformation of oleanolic acid by Alternaria longipes and Penicillium adametzi
Liu, Dai-Lin; Liu, Ying; Qiu, Feng; Gao, Ying; Zhang, Jing-Ze, Journal of Asian Natural Products Research, 2011, 13(2), 160-167

Rosamultin Raw materials

Rosamultin Preparation Products

Rosamultin Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:88515-58-6)Rosamultin
Order Number:A1205521
Stock Status:in Stock
Quantity:20mg/10mg
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 03:42
Price ($):150.0/237.0

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Amadis Chemical Company Limited
(CAS:88515-58-6)Rosamultin
A1205521
Purity:99%/99%
Quantity:20mg/10mg
Price ($):150.0/237.0
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