Home > Name List By s > Serpentine

CAS No 18786-24-8 , Serpentine

  • Name: Serpentine
  • CAS Registry Number:
  • EINECS: 242-570-5
  • Molecular Weight: 498.48
  • InChI: InChI=1/C21H20N2O3.C4H6O6/c1-12-16-10-23-8-7-14-13-5-3-4-6-18(13)22-20(14)19(23)9-15(16)17(11-26-12)21(24)25-2;5-1(3(7)8)2(6)4(9)10/h3-8,11-12,15-16H,9-10H2,1-2H3;1-2,5-6H,(H,7,8)(H,9,10)/t12-,15?,16?;/m0./s1
  • Molecular Formula: C25H26N2O9
  • Molecular Structure:CAS No:18786-24-8 Serpentine

Related products

Search by region :

Select to

18786-24-8 ALSTONINE

  • Germany Cfm Oskar Tropitzsch [Manufacturer]
  • Tel: +49-9231-9619-0
  • Fax: +49-9231-9619-60
  • Address: Cfm Oskar Tropitzsch
    Waldershofer Str. 49-51
    95615 Marktredwitz
    Germany null,nullGermany
Contact Supplier

18786-24-8 SERPENTINE HYDROGEN TARTRATE(RG)

  • SERPENTINE HYDROGEN TARTRATE(RG)Serpentine
  • United States ChromaDex Inc. [Manufacturer]
  • Tel: 949-419-0288
  • Fax: 949-419-0294
  • Address: ChromaDex Inc.
    10005 Muirlands Blvd. Suite G - First Floor
    Irvine, CA 92618 null,nullUnited States
Contact Supplier

18786-24-8 Serpentine

  • China BioBioPha Co., Ltd. [Manufacturer]
  • Tel: +86-871-5217109
  • Fax: +86-871-5217109
  • Address: 132 Lanhei Road, Kunming Institute of Botany, Chinese Academy of Sciences null,nullChina
Contact Supplier

18786-24-8 Serpentine hydrogen tartrate

  • Serpentine hydrogen tartrate
  • United States AvaChem Scientific LLC [Manufacturer]
  • Tel: 210-667-3815
  • Fax: 210-764-2240
  • Address: P.O.Box 78044278278 San Antonio, TexasUNITED STATES 78278 San Antonio, Texas,nullUnited States
Contact Supplier

18786-24-8 SERPENTINE

  • China FAITH EAGLE (LABORATORY) LTD. [Manufacturers]
  • Tel: (+86-755) 82851290
  • Fax: +86-755-83164680 83662918
  • Address: 15A/F.,Block A,World Trade Plaza,8# FuHong Rd., FuTian,Shenzhen, China Shenzhen,GuangdongChina
Contact Supplier

Select to

References of Serpentine
Title: Serpentine (Alkaloid)
CAS Registry Number: 18786-24-8
CAS Name: 3,4,5,6,16,17-Hexadehydro-16-(methoxycarbonyl)-19a-methyloxayohimbanium
Molecular Formula: C21H20N2O3
Molecular Weight: 348.40
Percent Composition: C 72.40%, H 5.79%, N 8.04%, O 13.78%
Literature References: From roots of Rauwolfia serpentina (L.) Benth., Apocynaceae: Schlittler, Schwarz, Helv. Chim. Acta 33, 1463 (1950). Structure: Schlittler et al., ibid. 37, 1912 (1954); Klohs et al., J. Am. Chem. Soc. 76, 1332 (1954); Wenkert, Roychaudhuri, ibid. 80, 1613 (1958). Stereoisomer of alstonine, q.v. Stereochemistry: Fritz, Ann. 655, 148 (1962); Shamma, Richey, J. Am. Chem. Soc. 85, 2507 (1963).
Properties: Solvated, yellow rods or leaflets from abs ethanol, mp 158° (air-dried), mp 175° (after drying at 120° in a high vacuum, but still not entirely solvent-free). Dec and turns red on drying at 150°. [a]D25 +292° (c = 0.27 in methanol); [a]D25 +267° (c = 0.21 in ethanol). uv max (ethanol): 252, 308, 370 nm (log e 4.49, 4.30, 3.61). Freely sol in methanol. Sol in 10% acetic acid, in other organic solvents.
Melting point: mp 158° (air-dried); mp 175° (after drying at 120° in a high vacuum, but still not entirely solvent-free)
Optical Rotation: [a]D25 +292° (c = 0.27 in methanol); [a]D25 +267° (c = 0.21 in ethanol)
Absorption maximum: uv max (ethanol): 252, 308, 370 nm (log e 4.49, 4.30, 3.61)
 
Derivative Type: Nitrate
Molecular Formula: C21H20N2O3.HNO3
Molecular Weight: 411.41
Percent Composition: C 61.31%, H 5.14%, N 10.21%, O 23.33%
Properties: Yellow crystals, mp 170-172°. Only slightly sol in water.
Melting point: mp 170-172°
 
Derivative Type: Hydrochloride monohydrate
Molecular Formula: C21H20N2O3.HCl.H2O
Molecular Weight: 402.87
Percent Composition: C 62.61%, H 5.75%, N 6.95%, O 15.89%, Cl 8.80%
Properties: Yellow crystals, mp 246-248°. [a]D23 +178°. Sol in water.
Melting point: mp 246-248°
Optical Rotation: [a]D23 +178°
 
Derivative Type: Perchlorate
Molecular Formula: C21H20N2O3.HClO4
Molecular Weight: 448.85
Percent Composition: C 56.19%, H 4.72%, N 6.24%, O 24.95%, Cl 7.90%
Properties: Yellow crystals, mp 255-256°. [a]D22 +185° (c = 0.5 in acetone). uv max (methanol): 252, 306-308, 365-370 nm (log e 4.54, 4.35, 3.68).
Melting point: mp 255-256°
Optical Rotation: [a]D22 +185° (c = 0.5 in acetone)
Absorption maximum: uv max (methanol): 252, 306-308, 365-370 nm (log e 4.54, 4.35, 3.68)