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Detail of "21887-01-4"

  • CAS Number:
  • 21887-01-4
  • Name:
  • 1,4-Phenanthrenedione,4b,5,6,7,8,8a,9,10-octahydro-3,10-dihydroxy-4b,8,8-trimethyl-2-(1-methylethyl)-,(4bS,8aS,10R)-

  • Molecular Structure:
  • Formula:
  • C20H28 O4
  • Molecular Weight:
  • 0
  • Synonyms:
  • 1,4-Phenanthrenedione,4b,5,6,7,8,8a,9,10-octahydro-3,10-dihydroxy-4b,8,8-trimethyl-2-(1-methylethyl)-,[4bS-(4ba,8ab,10b)]-; Horminone (7CI); Podocarpa-8,12-diene-11,14-dione, 7a,12-dihydroxy-13-isopropyl-(8CI); 7a-Hydroxyroyleanone; NSC 294577
  • Density:
  • 1.19g/cm3
  • Boiling Point:
  • 461.2°Cat760mmHg
  • Flash Point:
  • 246.9°C

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CAS No.21887-01-4 1,4-Phenanthrenedione,4b,5,6,7,8,8a,9,10-octahydro-3,10-dihydroxy-4b,8,8-trimethyl-2-(1-methylethyl)-,(4bS,8aS,10R)-

Assay:97.00%  Appearance:powder or cr...  Package:10mg,20mg,1g...Storage:-20degree  Transportation:room tempera...  Application:For research...

Supplier:shanghai Tauto Biotech Co., Ltd [ China (Mainland)]

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CAS No.21887-01-4 1,4-Phenanthrenedione,4b,5,6,7,8,8a,9,10-octahydro-3,10-dihydroxy-4b,8,8-trimethyl-2-(1-methylethyl)-,(4bS,8aS,10R)-

Supplier:Jamson Pharmachem Technology Co.,Ltd. [ China (Mainland)]

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CAS No.21887-01-4 1,4-Phenanthrenedione,4b,5,6,7,8,8a,9,10-octahydro-3,10-dihydroxy-4b,8,8-trimethyl-2-(1-methylethyl)-,(4bS,8aS,10R)-

Supplier:BBP [ China (Mainland)]

610Integral
610

Tel:+86-871-5217109

Address:132 Lanhei Road, Kunming Institute of Botany, Chinese Academy of Sciences

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Reference

A novel phenalenone from Salvia moorcraftiana
A novel phenalenone from Salvia moorcraftiana. Bakshi, Beena; Mulchandani, N. B.; Shankar, Jagdish (Cent.In this study, 6855-99-8 and 21887-01-4 are also used. Res. Dev., Univ. Kashmir, Kashmir 190006, India). Planta Med., (5), 408 (English) 1986. CODEN: PLMEAA. ISSN: 0032-0943. DOCUMENT TYPE: Journal CA Section: 11 (Plant Biochemistry) Section cross-reference(s): 26 The roots of sage (S. moorcraftiana) were extd. with C6H6, and 2 compds. were sepd. by chromatog. on silica gel and preparative TLC. The first of these was a phenalenone deriv. (I); its structure was detd. by physicochem. and spectral anal. In addn. a phenolic diterpenoid was obtained. Was also obtained by sulfuric acid treatment of 7a-hydroxyroyleanone or 6,7dehydroroyleanone. .
Diterpenoids from the roots of Mexican Salvia species
All Rights Reserved. Diterpenoids from the roots of Mexican Salvia species. Phytogeographical and evolutionary significance. Esquivel, Baldomero; Calderon, Jose S.; Arano, Maria Genoveva; Hernandez, Paola M.; Sanchez, Ana Adela (Instituto de Quimica de la Universidad Nacional Autonoma de Mexico, Circuito Exterior de Cd. Universitaria, Coyoacan 04510, Mex.). Revista Latinoamericana de Quimica, 33(2), 82-89 (English) 2005 Laboratorios Mixim S.A de C.V. CODEN: RLAQA8. ISSN: 0370-5943. DOCUMENT TYPE: Journal CA Section: 11 (Plant Biochemistry) Section cross-reference(s): 30 From the roots of Salvia candicans, S. tenoriana, S. pubescens, and S. lasiantha classified in Subgenus Jungia, several diterpenoids belonging to abietane, icetexane, totarane and 6-7-seco-abietane skeletons were isolated. Although these compds. were previously known from different sources, this is the first report on the diterpenoid constituents from the roots of these species. A reinvestigation of the roots of S. fruticosa is also described. The presence and phytogeog. 21887-01-4 and 88664-09-9 are just another two chemicals used in this study. distribution of these diterpenoids in the roots of the Mexican Salvia species studied up to now, suggest an evolutionary link between the Chinese and New World Salvias. .
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