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6-benzyloxy-2,3-dibromo-benzo[b]thiophene 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 648906-03-0 Structure
  • Basic information

    1. Product Name: 6-benzyloxy-2,3-dibromo-benzo[b]thiophene 1-oxide
    2. Synonyms: 6-benzyloxy-2,3-dibromo-benzo[b]thiophene 1-oxide
    3. CAS NO:648906-03-0
    4. Molecular Formula:
    5. Molecular Weight: 414.117
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 648906-03-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-benzyloxy-2,3-dibromo-benzo[b]thiophene 1-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-benzyloxy-2,3-dibromo-benzo[b]thiophene 1-oxide(648906-03-0)
    11. EPA Substance Registry System: 6-benzyloxy-2,3-dibromo-benzo[b]thiophene 1-oxide(648906-03-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 648906-03-0(Hazardous Substances Data)

648906-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 648906-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,8,9,0 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 648906-03:
(8*6)+(7*4)+(6*8)+(5*9)+(4*0)+(3*6)+(2*0)+(1*3)=190
190 % 10 = 0
So 648906-03-0 is a valid CAS Registry Number.

648906-03-0Relevant articles and documents

Structure-activity relationships of SERMs optimized for uterine antagonism and ovarian safety

Richardson, Timothy I.,Frank, Scott A.,Wang, Minmin,Clarke, Christian A.,Jones, Scott A.,Ying, Bai-Ping,Kohlman, Dan T.,Wallace, Owen B.,Shepherd, Timothy A.,Dally, Robert D.,Palkowitz, Alan D.,Geiser, Andrew G.,Bryant, Henry U.,Henck, Judith W.,Cohen, Ilene R.,Rudmann, Daniel G.,McCann, Denis J.,Coutant, David E.,Oldham, Samuel W.,Hummel, Conrad W.,Fong, Kin C.,Hinklin, Ronald,Lewis, George,Tian, Hongqi,Dodge, Jeffrey A.

, p. 3544 - 3549 (2008/02/07)

Structure-activity relationship studies are described, which led to the discovery of novel selective estrogen receptor modulators (SERMs) for the potential treatment of uterine fibroids. The SAR studies focused on limiting brain exposure and were guided by computational properties. Compounds with limited impact on the HPO axis were selected using serum estrogen levels as a biomarker for ovarian stimulation.

SELECTIVE ESTROGEN RECEPTOR MODULATORS CONTAINING A PHENYLSULFONYL GROUP

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Page/Page column 77-79, (2008/06/13)

The present invention relates to a selective estrogen receptor modulator of formula I or a pharmaceutical acid addition salt thereof; useful, e.g., for treating endometriosis and/or uterine leiomyoma/leiomyomata.

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