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(4-(2-Hydroxyethoxy)phenyl)(phenyl)methanone is an organic compound that serves as a crucial intermediate in the synthesis of various pharmaceuticals. It is characterized by its molecular structure, which includes a phenyl group and a hydroxyethoxy group, contributing to its unique chemical properties and reactivity.

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  • 14814-17-6 Structure
  • Basic information

    1. Product Name: (4-(2-hydroxyethoxy)phenyl)(phenyl)methanone
    2. Synonyms: (4-(2-hydroxyethoxy)phenyl)(phenyl)methanone;Methanone, [4-(2-hydroxyethoxy)phenyl]phenyl-
    3. CAS NO:14814-17-6
    4. Molecular Formula: C15H14O3
    5. Molecular Weight: 242.26986
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14814-17-6.mol
  • Chemical Properties

    1. Melting Point: 79-80 °C(Solv: heptane (142-82-5))
    2. Boiling Point: 421.0±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.178±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: Chloroform, Dichloromethane, DMSO, Methanol
    9. PKA: 14.14±0.10(Predicted)
    10. CAS DataBase Reference: (4-(2-hydroxyethoxy)phenyl)(phenyl)methanone(CAS DataBase Reference)
    11. NIST Chemistry Reference: (4-(2-hydroxyethoxy)phenyl)(phenyl)methanone(14814-17-6)
    12. EPA Substance Registry System: (4-(2-hydroxyethoxy)phenyl)(phenyl)methanone(14814-17-6)
  • 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: 14814-17-6(Hazardous Substances Data)

14814-17-6 Usage

Uses

Used in Pharmaceutical Industry:
(4-(2-Hydroxyethoxy)phenyl)(phenyl)methanone is used as an intermediate in the synthesis of E-Ospemifene (O703005) for its role in lowering serum cholesterol. E-Ospemifene, the E-isomer of Ospemifene (O703000), exhibits anti-atherosclerotic properties and has estrogen-like effects, making it a valuable compound in the development of treatments for conditions related to cholesterol and cardiovascular health.
Additionally, this compound may have potential applications in other areas of the pharmaceutical industry, depending on its specific chemical properties and reactivity, which could be further explored for the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 14814-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,1 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14814-17:
(7*1)+(6*4)+(5*8)+(4*1)+(3*4)+(2*1)+(1*7)=96
96 % 10 = 6
So 14814-17-6 is a valid CAS Registry Number.

14814-17-6SDS

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 [4-(2-hydroxyethoxy)phenyl]-phenylmethanone

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:14814-17-6 SDS

14814-17-6Relevant articles and documents

Synthesis of lithium ω-(m- and p-lithiophenoxy)alkoxides modified with magnesium 2-ethoxyethoxide. Crystal structures of bis[4-(2-hydroxyethoxy)phenyl]mercury and bis[4-(3-hydroxypropoxy)phenyl]mercury

Salteris, Constantinos S.,Kostas, Ioannis D.,Micha-Screttas, Maria,Steele, Barry R.,Heropoulos, George A.,Screttas, Constantinos G.,Terzis, Aris

, p. 63 - 70 (1999)

m- and p-Chlorinated ω-phenoxyalcohols 1, were transformed into the corresponding lithium ω-(m- and p-lithiophenoxy)alkoxides 4, respectively, by successive deprotonation with n-butyllithium and subsequent chlorine-lithium exchange by lithium naphthalene radical anion in THF-methylcyclohexane. Lithium 2-(4-lithiophenoxy)ethoxide (4a′) was also prepared by bromine-lithium exchange of 2-(4-bromophenoxy)ethanol (2a′) with two equivalents of n-butyllithium. The organolithiums were modified with magnesium 2-ethoxyethoxide in order to avoid ortho-metallation of the above-mentioned substituted arenes. Subsequent reaction of these intermediates with the electrophiles carbon dioxide, benzophenone, benzonitrile and 0.5 equivalents of mercuric chloride yielded the expected m- and p-substituted (ω-hydroxyalkoxy)benzenes in yields ranging from 50 to 75%. The crystal structures of the organomercurials 8a′ and 8b′ have been determined and revealed the Hg atom to occupy a crystallographic center of symmetry in a linear C-Hg-C arrangement.

Mechanically Robust, Self-Healable, and Highly Stretchable “Living” Crosslinked Polyurethane Based on a Reversible C?C Bond

Zhang, Ze Ping,Rong, Min Zhi,Zhang, Ming Qiu

, (2018)

Stimuli-responsive polymers built by reversible covalent bonds used to possess unbalanced mechanical properties. Here, a crosslinked polyurethane containing aromatic pinacol as a novel reversible C?C bond provider is synthesized, whose tensile strength an

METHOD FOR PREPARING HYDROXYBENZOPHENONE POLYGLYCOL ETHER (METH)ACRYLATE

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Paragraph 0061, (2020/08/30)

A method for preparing hydroxybenzophenone polyglycol ether (meth)acrylate comprising the steps of (i) reaction of hydroxybenzophenone with ethylene carbonate to give hydroxybenzophenone monoglycol ether,(ii) ethoxylation of hydroxybenzophenone monoglycol

A novel biocompatible zwitterionic polyurethane with AIE effect for cell imaging in living cells

Xu, Junhuai,Yan, Rui,Wang, Haibo,Du, Zongliang,Gu, Jun,Cheng, Xu,Xiong, Junjie

, p. 6798 - 6804 (2018/02/23)

In this work, a novel and stable zwitterionic polymer (TPE-CB PUs) was prepared to realize a cellular imaging system. TPE was conjugated into the backbone of zwitterionic polyurethane, which could be well dispersed in aqueous solution and emitted strong b

NITRILEOXIDE COMPOUND

-

Paragraph 0670; 0671; 0672, (2018/03/25)

The present invention provides a compound of the formula (I): wherein, R1 is a hydrogen atom or a hydrocarbon group; R2 is —R4—R5; R3 is —R4—R5 or —R4—R6; R

Polymorphic forms of the formulations (by machine translation)

-

Paragraph 0038; 0039; 0040;, (2017/04/07)

The present invention provides formulations, the chemical name (Z)- 2 - [4 - (4 - chloro - 1, 2 - diphenyl - d - 1 - enyl) phenoxy] ethanol polymorphic forms, it has excellent stability, and can be a reproduction of the crystal structure. In addition, the present invention also provides formulations polymorph forms of preparation method. (by machine translation)

Photoreactive oligoethylene glycol polymers - Versatile compounds for surface modification by thin hydrogel films

Buller, Jens,Laschewsky, Andre,Wischerhoff, Erik

, p. 929 - 937 (2013/03/13)

Solid surfaces are modified using photo-crosslinkable copolymers based on oligo(ethylene glycol) methacrylate (OEGMA) bearing 2-(4-benzoylphenoxy)ethyl methacrylate (BPEM) as a photosensitive crosslinking unit. Thin films of about 100 nm are formed by spi

NEW PROCESSES FOR PRODUCING BENZOPHENONE DERIVATIVES

-

Page/Page column 23, (2011/08/08)

There is provided a process for the preparation of a compound of formula (I): wherein X, R1, R2a, R2b, R2c, R2d, R2e, R3a, R3b, R3c, R3d and R3e are as described in the description. Such compounds may, for example, be useful medicament (or intermediates for medicaments).

Photochromic polymer conjugates: The importance of macromolecular architecture in controlling switching speed within a polymer matrix

Ercole, Francesca,Malic, Nino,Harrisson, Simon,Davis, Thomas P.,Evans, Richard A.

experimental part, p. 249 - 261 (2011/10/02)

Naphthopyran-poly(n-butyl acrylate) conjugates with different geometries were assembled using ATRP. First, within a rigid lens matrix, an investigation of the photochromic behavior of various poly(n-butyl acrylate), p(n-BA), homopolymers showed that midplacement of a single dye moiety, made possible using a Y-branching difunctional photochromic initiator, gave superior fade kinetics per chain length of conjugated polymer compared to end-functionalized homopolymers. Furthermore, having the dye pendant from the chain opposed to directly within the chain was also found to be advantageous. Fading kinetics became faster when chain length was increased, except in the case of linear random copolymers made by copolymerization of n-butyl acrylate with a naphthopyran acrylate. A gradient copolymer made with a nonphotochromic difunctional initiator and a naphthopyran methacrylate displayed superior kinetics. Films consisting of ABA triblock copolymers, incorporating the photochromic in the middle of a soft p(n-BA) section, gave slower switching speeds compared to lens samples, with responses that were highly tunable and dependent on the amount of soft section inhabited by the photochromic moiety.

AZIRIDINE-FUNCTIONAL PHOTOACTIVE CROSSLINKING COMPOUNDS

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Page/Page column 23, (2010/06/20)

A photoactive compound that is the Michael addition reaction product of an aziridine compound and a photoinitiator-functional (meth)acrylate is described. The compound can be used to crosslink (meth)acrylic polymers via a hydrogen abstracting or an alpha-

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