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CAS No 128-27-8 , Ergosta-5,7,22-trien-3-ol,(3b,10a,22E)- (9CI)

  • Name: Ergosta-5,7,22-trien-3-ol,(3b,10a,22E)- (9CI)
  • Synonyms: Pyroergocalciferol; 9a-Lumisterol; 10a-Ergosterol;10a-Ergosta-5,7,22-trien-3b-ol (7CI,8CI);Pyrovitamin D2;Ergosta-5,7,22-trien-3-ol,(3b,10a,22E)- (9CI); Pyrocalciferol(6CI);
  • CAS Registry Number:
  • Flash Point: 216.3°C
  • Boiling Point: 501.5°C at 760 mmHg
  • Density: 1g/cm3
  • Refractive index: 1.542
  • Flash Point: 216.3°C
  • Molecular Weight: 0
  • InChI: InChI=1/C28H44O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-10,18-20,22,24-26,29H,11-17H2,1-6H3/b8-7+/t19-,20+,22-,24+,25-,26-,27+,28+/m0/s1
  • Molecular Formula: C28H44 O

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References of Ergosta-5,7,22-trien-3-ol,(3b,10a,22E)- (9CI)
Title: Pyrocalciferol
CAS Registry Number: 128-27-8
CAS Name: (3b,10a,22E)-Ergosta-5,7,22-trien-3-ol
Synonyms: 9a-lumisterol; 9a-lumista-5,7,22-trien-3b-ol
Molecular Formula: C28H44O
Molecular Weight: 396.65
Percent Composition: C 84.78%, H 11.18%, O 4.03%
Literature References: Differs from ergosterol in the steric configuration at C-9 and C-10. Formation via isopyrocalciferol: Askew et al., Proc. Roy. Soc. London B109, 488 (1932); Windaus et al., Nachr. Ges. Wiss. Goettingen Math.-Phys. Kl. 1932, 150. Dehydrogenation with selenium gives Diel's hydrocarbon (3￠-methyl-1,2-cyclopentenophenanthrene). Fieser, Fieser, Steroids (New York, 1959) pp 136-143, argue the configuration at C-9 and C-10. See also Castells et al., J. Chem. Soc. 1959, 1159. Critical examination and comparison with other unnatural steroids: Castells et al., ibid. 1962, 2907.
Properties: Needles from methanol, mp 93-95°. [a]D20 +512°, [a]20546 +624° (c = 0.15 in alcohol). uv max: 274, 294 nm (Askew).
Melting point: mp 93-95°
Optical Rotation: [a]D20 +512°; [a]20546 +624° (c = 0.15 in alcohol)
Absorption maximum: uv max: 274, 294 nm (Askew)
 
Derivative Type: Acetate
Molecular Formula: C30H46O2
Molecular Weight: 438.69
Percent Composition: C 82.14%, H 10.57%, O 7.29%
Properties: mp 81-82°, [a]D +403° (chloroform).
Melting point: mp 81-82°
Optical Rotation: [a]D +403° (chloroform)
 
Derivative Type: 3,5-Dinitrobenzoate
Molecular Formula: C35H46N2O6
Molecular Weight: 590.75
Percent Composition: C 71.16%, H 7.85%, N 4.74%, O 16.25%
Properties: mp 168-170°. [a]D21 +195°, [a]20546 +249° (both c = 2 in chloroform).
Melting point: mp 168-170°
Optical Rotation: [a]D21 +195°; [a]20546 +249° (both c = 2 in chloroform)