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CAS No 130-79-0 , Benzene,1,1'-[(1E)-1,2-diethyl-1,2-ethenediyl]bis[4-methoxy-

  • Name: Benzene,1,1'-[(1E)-1,2-diethyl-1,2-ethenediyl]bis[4-methoxy-
  • Synonyms: Diethylstilbestrol dimethyl ether; trans-3,4-Di-p-anisyl-3-hexene; Stilbene, a,a'-diethyl-4,4'-dimethoxy-, trans- (4CI); Depot-Oestromenin;Depot-Cyren; Dimestrol;Benzene,1,1'-[(1E)-1,2-diethyl-1,2-ethenediyl]bis[4-methoxy-;Depot-Oestrromon; Oestrastilben (D); E-3,4-Dianisyl-3-hexene; Stilbestroldimethyl ether; Depot-Oestromenine; Depot-Oestromon; Stilbene, a,a'-diethyl-4,4'-dimethoxy-, (E)- (8CI); Depoestron; Estromenin-Deposito; EstrastilbeneD;Dimethoxydiethylstilbestrol; Oestromenine-Depot; Synthila; Dimoestrol;Benzene,1,1'-(1,2-diethyl-1,2-ethenediyl)bis[4-methoxy-, (E)-;
  • CAS Registry Number:
  • Flash Point: 134.6°C
  • Boiling Point: 390.7°Cat760mmHg
  • Density: 0.999g/cm3
  • Refractive index: 1.545
  • Flash Point: 134.6°C
  • EINECS: 204-994-9
  • Molecular Weight: 296.4
  • InChI: InChI=1/C20H24O2/c1-5-19(15-7-11-17(21-3)12-8-15)20(6-2)16-9-13-18(22-4)14-10-16/h7-14H,5-6H2,1-4H3/b20-19+
  • Molecular Formula: C20H24 O2
  • Molecular Structure:CAS No:130-79-0 Benzene,1,1'-[(1E)-1,2-diethyl-1,2-ethenediyl]bis[4-methoxy-

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References of Benzene,1,1'-[(1E)-1,2-diethyl-1,2-ethenediyl]bis[4-methoxy-
Title: Dimestrol
CAS Registry Number: 130-79-0
CAS Name: 1,1￠-[(1E)-1,2-Diethyl-1,2-ethenediyl]bis[4-methoxybenzene]
Synonyms: (E)-a,a￠-diethyl-4,4￠-dimethoxystilbene; stilbestrol dimethyl ether; (E)-3,4-bis(p-methoxyphenyl)-3-hexene; (E)-3,4-dianisyl-3-hexene
Molecular Formula: C20H24O2
Molecular Weight: 296.40
Percent Composition: C 81.04%, H 8.16%, O 10.80%
Literature References: Nonsteroidal synthetic estrogen; dimethyl ether of diethylstilbestrol, q.v. Prepn: Dodds et al., Nature 142, 211, 247 (1938); Reid, Wilson, J. Am. Chem. Soc. 64, 1625 (1942); Sisido, Nozaki, J. Am. Chem. Soc. 70, 777 (1948). Improved stereospecific prepn: T. Hiyama, H. Nozaki, Bull. Chem. Soc. Jpn. 46, 2248 (1973). Crystal structure: G. Ruban, P. Luger, Acta Crystallogr. B31, 2658 (1975). Biological activities: Y. Inamori et al., Chem. Pharm. Bull. 33, 4478 (1985). Review and bibliography: Solmssen, Chem. Rev. 37, 481 (1945).
Properties: Crystals from petr ether, mp 124°. Less sol than the monomethyl ether, mestilbol. Practically insol in water. Sol in alcohol; freely sol in acetone, ether; also sol in dil aq or alcoholic solns of alkali hydroxides and in vegetable oils.
Melting point: mp 124°