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3-[(1-Methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acid is a chemical compound that belongs to the class of benzoic acids. It features a benzoic acid backbone with two distinct side chains, one with an isopropyl group and the other with a phenylmethyl group. 3-[(1-Methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acid exhibits potential biological activities and is valuable in medicinal chemistry for the development of drugs and pharmaceuticals.

852520-53-7

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852520-53-7 Usage

Uses

Used in Medicinal Chemistry:
3-[(1-Methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acid is used as a building block for the development of drugs and pharmaceuticals due to its potential biological activities.
Used in Research Laboratories:
In research settings, 3-[(1-Methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acid is utilized for various studies related to organic chemistry and drug discovery, contributing to the advancement of scientific knowledge in these fields.
Used in Industrial Applications:
3-[(1-Methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acid may also have industrial applications, particularly in the synthesis of other chemicals or materials, broadening its use beyond the laboratory and medicinal contexts.

Check Digit Verification of cas no

The CAS Registry Mumber 852520-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,5,2 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 852520-53:
(8*8)+(7*5)+(6*2)+(5*5)+(4*2)+(3*0)+(2*5)+(1*3)=157
157 % 10 = 7
So 852520-53-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H18O4/c1-12(2)21-16-9-14(17(18)19)8-15(10-16)20-11-13-6-4-3-5-7-13/h3-10,12H,11H2,1-2H3,(H,18,19)

852520-53-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylmethoxy-5-propan-2-yloxybenzoic acid

1.2 Other means of identification

Product number -
Other names 3-[(1-methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acid

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:852520-53-7 SDS

852520-53-7Relevant academic research and scientific papers

IMIDAZOPYRIDINE COMPOUNDS

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Page/Page column 23, (2010/04/23)

Compounds, pharmaceutical compositions, kits and methods are provided for use with glucokinase that comprise a compound selected from the group consisting of formula (I) wherein the variables are as defined herein.

N- ( PYRAZOLE- 3 -YL) -BENZAMIDE DERIVATIVES AS GLUCOKINASE ACTIVATORS

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Page/Page column 46-47, (2009/05/30)

Novel heterocyclic compounds of the formula (I) in which R1, R2, R3, R4, R5, R6, R7, Alk and D have the meanings indicate in Claim 1, are activators of glucokinase and can be used for the prevention and/or treatment of Diabetes Typ 1 and 2, obesity, neuropathy and/or nephropathy.

THERAPEUTIC COMPOUNDS

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Page/Page column 69-70, (2010/11/27)

This invention relates to a novel class of substituted amino-ethoxy benzene derivatives of formula (I) which are inhibitors of serine proteases and to their use in treating aberrant serine protease activity in a mammal, contraception, anti-coagulant methods and methods for treating aberrant cell proliferation, tumours, cancer, angiogenesis, angiogenesis-based retinopathies, autoimmummune disease, inflammation, skin disease, arthritis, rheutmatoid arthritis, asthma, osteoarthritis and multiple sclerosis. (I), Wherein Rm, Rn, Rp, Rq, V, W, X, Y and R8 are as defined in the claims.

2 -HETEROCYCLYLOXYBENZOYL AMINO HETEROCYCLYL COMPOUNDS AS MODULATORS OF GLUCOKINASE FOR THE TREATMENT OF TYPE 2 DIABETES

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Page/Page column 54, (2010/11/25)

Compounds of formula (I) wherein R1, HET-1 and HET-2 are as described in the specification, and their salts, are activators of glucokinase (GLK) and are thereby useful in the treatment of, for example, type 2 diabetes. Processes for preparing compounds of formula (I) are also described.

HETEROARYL BENZAMIDE DERIVATIVES FOR USE AS GLK ACTIVATORS IN THE TREATMENT OF DIABETES

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Page/Page column 93, (2008/06/13)

Compounds of formula (I), wherein R1, R4, HET-1 and HET-2 are as described in the specification, and their salts and pro-drugs, are activators of glucokinase (GLK) and are thereby useful in the treatment of, for example, type 2 diabetes. Processes for preparing compounds of formula (I) are also described.

2-PHENYL SUBSTITUTED IMIDAZOL [4 , 5B] PYRIDINE/ PYRAZINE AND PURINE DERIVATIVES AS GLUCOKINASE MODULATORS

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Page/Page column 87, (2010/11/25)

Compounds of Formula (I), wherein R1- R10, A and X1 to X3 are as described in the specification, and their salts and pro-drugs, are activators of glucokinase (GLK) and are thereby useful in the treatment of, for example, type 2 diabetes. Processes for preparing compounds of formula (I) are also described.

Discovery, synthesis and biological evaluation of novel glucokinase activators

McKerrecher, Darren,Allen, Joanne V.,Bowker, Suzanne S.,Boyd, Scott,Caulkett, Peter W. R.,Currie, Gordon S.,Davies, Christopher D.,Fenwick, Mark L.,Gaskin, Harold,Grange, Emma,Hargreaves, Rod B.,Hayter, Barry R.,James, Roger,Johnson, Keith M.,Johnstone, Craig,Jones, Clifford D.,Lackie, Sarah,Rayner, John W.,Walker, Rolf P.

, p. 2103 - 2106 (2007/10/03)

The identification, synthesis and SAR of a novel series of glucokinase activators is described. The interplay between lipophilicity, potency and physical properties is discussed, and compound 22 highlighted as having a suitable balance. In vivo pharmacoki

BENZOYL AMINO PYRIDYL CARBOXYLIC ACID DERIVATIVES USEFUL AS GLUCOKINASE (GLK) ACTIVATORS

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Page/Page column 30-31, (2010/02/12)

Compounds of Formula: (I); wherein: R1 is selected from: fluoro, chloro, C1-3alkyl and C1-3alkoxy; R2-X- is selected from: methyl, methoxymethyl and Formula: (X); n is 0,1 or 2; or a salt, pro-drug or solvate thereof are described. Their use as GLK activators, pharmaceutical compositions containing them, and processes for their preparation are also described.

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