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Ethanone, 1-[2-hydroxy-5-methoxy-4-(phenylmethoxy)phenyl]-, is a complex chemical compound characterized by a ketone group attached to a substituted biphenyl ring. Ethanone, 1-[2-hydroxy-5-methoxy-4-(phenylmethoxy)phenyl]features a hydroxy group, a methoxy group, and a phenylmethoxy group, all of which are positioned on the biphenyl ring. It is likely a derivative of bisphenol A, an industrial chemical known for its estrogenic properties. The presence of these functional groups suggests potential interactions with biological systems, which may influence hormonal regulation or other physiological processes. Further research is necessary to fully comprehend the properties and potential applications of Ethanone, 1-[2-hydroxy-5-methoxy-4-(phenylmethoxy)phenyl]-.

34176-18-6

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34176-18-6 Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-[2-hydroxy-5-methoxy-4-(phenylmethoxy)phenyl]-, is used as a pharmaceutical candidate for its potential hormonal regulation properties. The presence of hydroxy and methoxy groups in the compound may allow it to interact with biological systems, potentially affecting hormonal balance and other physiological processes. Further research is required to explore its therapeutic applications and efficacy.
Used in Chemical Research:
Ethanone, 1-[2-hydroxy-5-methoxy-4-(phenylmethoxy)phenyl]is utilized in chemical research for studying the properties and behavior of complex organic molecules, particularly those with multiple functional groups. Its structure and potential interactions with biological systems make it an interesting subject for investigation in the field of organic chemistry and related disciplines.
Used in Material Science:
Ethanone, 1-[2-hydroxy-5-methoxy-4-(phenylmethoxy)phenyl]-, may be employed in material science for the development of new materials with specific properties. Ethanone, 1-[2-hydroxy-5-methoxy-4-(phenylmethoxy)phenyl]-'s unique structure and functional groups could contribute to the creation of novel materials with applications in various industries, such as electronics, coatings, or adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 34176-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,7 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34176-18:
(7*3)+(6*4)+(5*1)+(4*7)+(3*6)+(2*1)+(1*8)=106
106 % 10 = 6
So 34176-18-6 is a valid CAS Registry Number.

34176-18-6SDS

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 1-(4-benzyloxy-2-hydroxy-5-methoxy-phenyl)-ethanone

1.2 Other means of identification

Product number -
Other names 1-(4-Benzyloxy-2-hydroxy-5-methoxy-phenyl)-aethanon

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:34176-18-6 SDS

34176-18-6Relevant academic research and scientific papers

Structure Optimization of Gatastatin for the Development of γ-Tubulin-Specific Inhibitor

Chinen, Takumi,Ebisu, Haruna,Hatanaka, Taisei,Hayakawa, Ichiro,Mukaiyama, Minagi,Nagumo, Yoko,Sakakura, Akira,Shintani, Kana,Takao, Daisuke,Usui, Takeo

supporting information, p. 1125 - 1129 (2020/07/04)

Gatastatin (O7-benzyl glaziovianin A) is a γ-tubulin-specific inhibitor that is used to investigate γ-tubulin function in cells. We have previously reported that the unsubstituted phenyl ring of the O7-benzyl group in gatastatin is important for γ-tubulin

γ-TUBULIN INHIBITOR

-

Paragraph 0058-0061, (2020/03/27)

To provide a novel compound with a microtubule polymerization inhibitory activity promising as an anticancer agent.SOLUTION: The invention provides a compound represented by formula (I) in the figure or a pharmaceutically acceptable salt thereof.

2-OXO-5H-CHROMENO[4,3-B]PYRIDINES FOR USE IN THE TREATMENT OF HEPATITIS B

-

, (2019/06/23)

The present invention discloses compounds according to Formula (I), wherein R1, R2a, R2b, R3, R4, and R5 are as defined herein. The present invention relates to compounds, methods for their production, pharmaceutical compositions comprising the same, and methods of treatment using the same, for the prophylaxis and/or treatment of diseases involving hepatitis B by administering the compound of the invention.

Gastroprotective flavone/flavanone compounds with therapeutic effect on inflammatory bowel disease

-

, (2008/06/13)

PCT No. PCT/KR97/00144 Sec. 371 Date Jan. 14, 1999 Sec. 102(e) Date Jan. 14, 1999 PCT Filed Jul. 25, 1997 PCT Pub. No. WO98/04541 PCT Pub. Date Feb. 5, 1998The present invention relates to novel flavone/flavanone compounds or their pharmaceutically acceptable salts and process for preparation thereof for protecting gastrointestinal tracts against gastritis, ulcers and inflammatory bowel disease.

Structure-activity requirements for flavone cytotoxicity and binding to tubulin

Beutler, John A.,Hamel, Ernest,Vlietinck, Arnold J.,Haemers, Achiel,Rajan, Padinchare,Roitman, James N.,Cardellina II, John H.,Boyd, Michael R.

, p. 2333 - 2338 (2007/10/03)

A series of 79 flavones related to centaureidin (3,6,4'-trimethoxy- 5,7,3'-trihydroxyflavone, 1) was screened for cytotoxicity in the NCI in vitro 60-cell line human tumor screen. The resulting cytotoxicity profiles of these flavones were compared for deg

Structural Elucidation of Two New Chromones Isolated from Glasswort (Salicornia europaea L.)

Arakawa, Yoshihito,Chiji, Hideyuki,Izawa, Masao

, p. 2029 - 2034 (2007/10/02)

Two chromones isolated from the methanol extract of glasswort (Salicornia europaea L.) were elucidated to be 7-hydroxy-6-methoxychromone and 7-O-β-D-glucopyranosyl-6-methoxychromone on the basis of chemical and spectral analyses and synthetic studies.These two are natural products hitherto unknown.

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