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117113-98-1

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117113-98-1 Usage

General Description

4-(4-Fluorobenzyloxy)benzyl Alcohol is a specific category of synthetic chemicals formed through the complex process of organic synthesis. It is primarily utilized in the field of scientific research and development, often within the framework of pharmacological or biomedical investigations. Its structure consists of a benzyl alcohol derivative, characterized by an additional benzyl group attached to the alcoholic OH group. The primary feature of this unique structure is the presence of a Fluorine atom, which greatly contributes to its potential use in the development of Fluorine-based drugs. Despite its sophisticated structure, it is essential to handle and dispose of this chemical safely to prevent any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 117113-98-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,1 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 117113-98:
(8*1)+(7*1)+(6*7)+(5*1)+(4*1)+(3*3)+(2*9)+(1*8)=101
101 % 10 = 1
So 117113-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H13FO2/c15-13-5-1-12(2-6-13)10-17-14-7-3-11(9-16)4-8-14/h1-8,16H,9-10H2

117113-98-1 Well-known Company Product Price

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  • Alfa Aesar

  • (44022)  4-(4-Fluorobenzyloxy)benzyl alcohol, 98%   

  • 117113-98-1

  • 5g

  • 1764.0CNY

  • Detail
  • Alfa Aesar

  • (44022)  4-(4-Fluorobenzyloxy)benzyl alcohol, 98%   

  • 117113-98-1

  • 25g

  • 7066.0CNY

  • Detail

117113-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[(4-fluorophenyl)methoxy]phenyl]methanol

1.2 Other means of identification

Product number -
Other names 4-(4-FLUOROBENZYLOXY)BENZYL ALCOHOL

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:117113-98-1 SDS

117113-98-1Relevant articles and documents

Sophoridine pyrrole, indole derivative and preparation method and application thereof

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Paragraph 0191; 0193; 0196; 0202, (2018/09/08)

The invention relates to a sophoridine pyrrole, indole derivative. The invention discloses a chemical structure of the compound and further discloses a preparation method of the compound. In vitro anti-tumor activity researches show that anti-tumor drugs

Discovery of novel 3-benzylquinazolin-4(3H)-ones as potent vasodilative agents

Zuo, Sai-Jie,Li, Sen,Yu, Rui-Hong,Zheng, Guo-Xun,Cao, Yong-Xiao,Zhang, San-Qi

supporting information, p. 5597 - 5601 (2015/01/08)

In the present study, a series of 3-benzylquinazolin-4(3H)-ones were synthesized and characterized. Their vasodilative effects were evaluated by wire myograph on isolated rat mesenteric arterial ring induced contraction with 60 mM KCl. The SAR of target compounds was discussed preliminarily. Among these compounds, 2a and 2c displayed potent vasodilatation action and could compete significantly the rat mesenteric arterial rings induced contraction with phenylephrine. Compounds 2a and 2c were further tested for their antihypertensive effects in SHR by oral administration. The results indicated that 2a and 2c could reduce significantly both diastolic and systolic blood pressure. Moreover, 2c displayed antihypertensive effect in a dose dependent manner, and could maintain the effects for 6 h at a dosage of 4.0 mg/kg. These findings suggest that the title compounds are novel vasodilative agents, representing a novel series of promising antihypertensive agents.

Compounds that modulate PPAR activity and methods for their preparation

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Page 57, (2010/02/05)

This invention discloses compounds that alter PPAR activity. The invention also discloses pharmaceutically acceptable salts of the compounds, pharmaceutically acceptable compositions comprising the compounds or their salts, and methods of using them as therapeutic agents for treating or preventing disipidemia, hypercholesteremia, obesity, eating disorders, hyperglycemia, atherosclerosis, hypertriglyceridemia, hyperinsulinemia and diabetes in a mammal as well as methods of supressing appetite and modulating leptin levels in a mammal. The present invention also discloses methods for making the disclosed compounds.

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