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  • 341524-89-8 Structure
  • Basic information

    1. Product Name: 2-[2-[(Z)-4-chloro-1,2-diphenyl-but-1-enoxy]ethoxy]ethanol
    2. Synonyms: 2-[2-[(Z)-4-chloro-1,2-diphenyl-but-1-enoxy]ethoxy]ethanol;fispemifene;Ospemifene Impurity 1 (Fispemifene)
    3. CAS NO:341524-89-8
    4. Molecular Formula: C26H27ClO3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 341524-89-8.mol
    9. Article Data: 5
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 512.2°C at 760 mmHg
    3. Flash Point: 263.5°C
    4. Appearance: /
    5. Density: 1.156g/cm3
    6. Vapor Pressure: 2.59E-11mmHg at 25°C
    7. Refractive Index: 1.571
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-[2-[(Z)-4-chloro-1,2-diphenyl-but-1-enoxy]ethoxy]ethanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-[2-[(Z)-4-chloro-1,2-diphenyl-but-1-enoxy]ethoxy]ethanol(341524-89-8)
    12. EPA Substance Registry System: 2-[2-[(Z)-4-chloro-1,2-diphenyl-but-1-enoxy]ethoxy]ethanol(341524-89-8)
  • 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: 341524-89-8(Hazardous Substances Data)

341524-89-8 Usage

Description

2-[2-[(Z)-4-chloro-1,2-diphenyl-but-1-enoxy]ethoxy]ethanol is a complex organic compound characterized by its unique molecular structure. It is a derivative of phenylbutene, featuring a chloro group and multiple ethoxy groups, which contribute to its chemical properties and potential applications.

Uses

Used in Pharmaceutical Industry:
2-[2-[(Z)-4-chloro-1,2-diphenyl-but-1-enoxy]ethoxy]ethanol is used as an active pharmaceutical ingredient for the treatment of male hypogonadism and male urinary tract symptoms. Its chemical structure allows it to interact with specific receptors in the body, helping to alleviate symptoms and improve overall health.
Used in Hormonal Regulation:
In the field of endocrinology, 2-[2-[(Z)-4-chloro-1,2-diphenyl-but-1-enoxy]ethoxy]ethanol is used as a selective estrogen receptor modulator (SERM) for the treatment of androgen deficiency and the maintenance of hormonal estrogen levels. Its ability to modulate estrogen receptor activity makes it a valuable tool in managing hormone-related conditions and maintaining overall hormonal balance.

Check Digit Verification of cas no

The CAS Registry Mumber 341524-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,1,5,2 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 341524-89:
(8*3)+(7*4)+(6*1)+(5*5)+(4*2)+(3*4)+(2*8)+(1*9)=128
128 % 10 = 8
So 341524-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H23ClO3/c21-12-11-19(17-7-3-1-4-8-17)20(18-9-5-2-6-10-18)24-16-15-23-14-13-22/h1-10,22H,11-16H2/b20-19-

341524-89-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name fispemifene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:341524-89-8 SDS

341524-89-8Downstream Products

341524-89-8Relevant articles and documents

METHODS FOR IMMUNOMODULATION OF CANCER AND INFECTIOUS DISEASE THERAPY

-

Paragraph 0198, (2016/07/27)

The present invention provides methods for modulating the immune response of a subject to a therapeutic agent, the method comprising administering an effective amount of a triphenyl ethylene (TRIP) compound with an effective amount of the therapeutic agent. In particular embodiments, the TRIP compound enhances the immune response of the subject to the therapeutic agent. In some embodiments, the TRIP compound is administered in different dosing schedules to provide a biphasic immunomodulation effect.

METHOD FOR THE PREPARATION OF THERAPEUTICALLY VALUABLE TRIPHENYLBUTENE DERIVATIVES

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Page/Page column 3-4, (2008/12/08)

The present invention concerns a method for the preparation of therapeutically valuable triphenylbutene derivatives, especially ospemifene or fispemifene.

Triphenylalkene derivatives and their use as selective estrogen receptor modulators

-

, (2008/06/13)

The invention provides novel selective estrogen receptor modulator compounds of the general formula: wherein R1 and R2, which are the same or different are a) H, halogen, OCH3, OH; or ?where X is O, NH or S; and n is an integer from 1 to 4; and R4 and R5, which are the same or different, are a 1 to 4 carbon alkyl, H, —CH2C≡CH or —CH2CH2OH; or R4 and R5 form an N-containing five- or six-membered ring or heteroaromatic ring; or c) —Y—(CH2)nCH2—O—R6 where Y is O, NH or S and n is an integer from 1 to 4; and R6 is H, —CH2CH2OH, or —CH2CH2Cl; or d) 2,3-dihydroxypropoxy, 2-methylsulfamylethoxy, 2-chloroethoxy, 1-ethyl-2-hydroxyethoxy, 2,2-diethyl-2-hydroxyethoxy or carboxymethoxy; and R3 is H, halogen, OH or —OCH3; stereoisomers thereof and their non-toxic pharmaceutically acceptable salts and esters and mixtures thereof, which compounds exhibit valuable pharmacological properties.

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