Home > Name List By b > Brassinolide India

CAS No 72962-43-7 , Brassinolide Search by region : India

  • Name: Brassinolide
  • Synonyms: 72962-43-7; 2alpha,3alpha,22alpha,23alpha-Tetrahydroxy-24alpha-methyl-B-homo-7-oxa-5alpha-cholestan-6-one;24-Epibrassinolide;Brassinolide;
  • CAS Registry Number:
  • Flash Point: 633.7 ºC at 760 mmHg
  • Boiling Point: 633.7 ºC at 760 mmHg
  • Density: 1.141 g/cm3
  • Flash Point: 633.7 ºC at 760 mmHg
  • Molecular Weight: 480.67712
  • InchiKey: IXVMHGVQKLDRKH-KNBKMWSGSA-N
  • InChI: InChI=1S/C28H48O6/c1-14(2)15(3)24(31)25(32)16(4)18-7-8-19-17-13-34-26
    (33)21-11-22(29)23(30)12-28(21,6)20(17)9-10-27(18,19)5/h14-25,29-32H,
    7-13H2,1-6H3/t15-,16-,17-,18+,19-,20-,21+,22-,23+,24+,25+,27+,28+/m0/s1
  • Molecular Formula: C28H48O6
  • Molecular Structure:CAS No:72962-43-7 Brassinolide

Related products

Select to

72962-43-7 Brassinolide

  • India Manus Aktteva null
  • Tel: +91-(79)-65123395
  • Fax: +91-(79)-26463395
  • Address: 303, 3rd Floor, Royale Manor, Law Garden, Dhulia Kot Road, Ellisbridge, Ahmedabad, Gujarat 380006, null,nullIndia
Contact Supplier

72962-43-7 6H-Benz[c]indeno[5,4-e]oxepin-6-one,1-[(1S,2R,3R,4S)-2,3-dihydroxy-1,4,5-trimethylhexyl]hexadecahydro-8,9-dihydroxy-10a,12a-dimethyl-,(1R,3aS,3bS,6aS,8S,9R,10aR,10bS,12aS)-

  • India ACM Chemicals [Manufacturers]
  • Tel: +91-(265)-9428762088
  • Fax: +91-
  • Address: A/90-Natasha park - 2, Nzp Rd, Vadodara, Gujarat 390002, BARODA,GujaratIndia
Contact Supplier

Select to

References of Brassinolide
Title: Brassinolide
CAS Registry Number: 72962-43-7
CAS Name: (2a,3a,5a,22R,23R,24S)-2,3,22,23-Tetrahydroxy-B-homo-7-oxaergostan-6-one
Synonyms: 2a,3a,22,23-tetrahydroxy-24-methyl-B-homo-7-oxa-5a-cholestan-6-one
Molecular Formula: C28H48O6
Molecular Weight: 480.68
Percent Composition: C 69.96%, H 10.07%, O 19.97%
Literature References: Plant hormone; natural steroid containing a seven-membered B-ring lactone, that promotes both cell elongation and cell division. Over ten brassinosteroids have been isolated and characterized from sources such as pollen, seedling, leaf. Isoln, structure and activity of brassinolide from rape pollen, Brassica napus L.: M. D. Grove et al., Nature 281, 216 (1979). Stereoselective synthesis: S. Fung, J. B. Siddall, J. Am. Chem. Soc. 102, 6580 (1980). Synthesis of two stereoisomers: M. J. Thompson et al., J. Org. Chem. 44, 5002 (1979). Improved synthesis: T. Kametani et al., J. Org. Chem. 53, 1982 (1988). Structure-activity relationship of brassinosteroids: S. Takatsuto et al., Phytochemistry 22, 2437 (1983); interaction with cytokinin: C. Schlagnhaufer et al., Physiol. Plant. 60, 347 (1984); bioassay: K. Wada et al., Agric. Biol. Chem. 48, 719 (1984).
Properties: Crystals from methanol, mp 274-275°. [a]D27 +16°.
Melting point: mp 274-275°
Optical Rotation: [a]D27 +16°
Use: Plant growth regulator.