Estrone 3-methyl etherEstrone 3-methyl ether - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-79576-01.804-HY-79576-01804-HY-79576-01Business & Industrial > Science & LaboratoryEstrone 3-methyl ether
Gentaur
EUR12027-02-25

Estrone 3-methyl ether

CAT:
804-HY-79576-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Estrone 3-methyl ether - image 1

Estrone 3-methyl ether

  • Description:

    Estrone 3-methyl ether (Oestrone methyl ether; 3-O-Methylestrone) is a synthetic intermediate useful for synthesis of estrogen receptor modulator[1][2][3].
  • Product Name Alternative:

    Oestrone methyl ether; 3-O-Methylestrone
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302, H315, H319, H335
  • Target:

    Drug Intermediate
  • Related Pathways:

    Others
  • Field of Research:

    Cancer
  • Purity:

    98.82
  • Solubility:

    DMSO : 4.17 mg/mL (ultrasonic; warming; heat to 60°C)
  • Smiles:

    C[C@@]12[C@](CCC2=O)([H])[C@@]3([H])[C@@](CC1)([H])C4=CC=C(OC)C=C4CC3
  • Molecular Formula:

    C19H24O2
  • Molecular Weight:

    284.39
  • Precautions:

    H302, H315, H319, H335
  • References & Citations:

    [1]Kuznetsov YV, et al. New estrogen receptor antagonists. 3,20-Dihydroxy-19-norpregna-1,3,5 (10) -trienes: Synthesis, molecular modeling, and biological evaluation. Eur J Med Chem. 2018 Jan 1;143:670-682.|[2]Herman BE, et al. Comparative investigation of the in vitro inhibitory potencies of 13-epimeric estrones and D-secoestrones towards 17β-hydroxysteroid dehydrogenase type 1. J Enzyme Inhib Med Chem. 2016;31 (sup3) :61-69.|[3]Kuznetsov YV, et al. New estrogen receptor antagonists. 3,20-Dihydroxy-19-norpregna-1,3,5 (10) -trienes: Synthesis, molecular modeling, and biological evaluation. Eur J Med Chem. 2018 Jan 1;143:670-682.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    No Development Reported
  • CAS Number:

    [1624-62-0]