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58530-50-0

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58530-50-0 Usage

General Description

(2-Pyridinyloxy)acetic acid is a chemical compound that is part of the pyridine and carboxylic acid classes. The pyridine ring in the compound contributes to its basicity and ability to participate in various chemical reactions. It is often used in scientific research due to its unique chemical structure and properties. Additionally, it can serve as a pharmaceutical intermediate. Its molecular formula is C7H7NO3, and it has a molar mass of 153.14 g/mol. It exhibits an aromatic character, which means it has a unique stability compared to other types of compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 58530-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,3 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58530-50:
(7*5)+(6*8)+(5*5)+(4*3)+(3*0)+(2*5)+(1*0)=130
130 % 10 = 0
So 58530-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO3/c9-7(10)5-11-6-3-1-2-4-8-6/h1-4H,5H2,(H,9,10)

58530-50-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyridin-2-yloxyacetic acid

1.2 Other means of identification

Product number -
Other names pyridyloxyacetic 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:58530-50-0 SDS

58530-50-0Downstream Products

58530-50-0Relevant articles and documents

Design of a Synthetic Foldamer that Modifies the Growth of Calcite Crystals

Estroff, Lara A.,Incarvito, Christopher D.,Hamilton, Andrew D.

, p. 2 - 3 (2004)

An oligopyridine foldamer, whose structure is dictated by bifurcated hydrogen bonds, was designed to recognize the surface of calcite through three carboxylates, projected from one face of the molecule. At low concentrations of the trimer, elongated calcite crystals with angular, teeth-like growths, identified as {↑0l} faces, were exclusively formed. In the presence of a related monomer, only calcite rhombohedra are formed, indicating that it is the ordered array of carboxylates that causes the morphological changes, via a specific interaction between the foldamer and the newly expressed faces of the growing calcite crystals. Copyright

Phenylazole compounds, process for producing the same and drugs for hyperlipemia

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Example 7, (2008/06/13)

Phenylazole compounds represented by general formula (1) or pharmaceutically acceptable salts thereof and drugs for hyperlipemia which contain these compounds as the active ingredient, wherein A represents imidazolyl, pyrazolyl, etc.; B represents (1a) or (1b) (wherein R2and R3represent each hydrogen, C1-6alkyl, etc; and k is 0 or an integer of 1 to 15); Y represents O, S, a bond, etc.; and Z represents an optionally substituted and saturated or unsaturated heterocycle containing 1 to 4 N, O or S atoms. Among all, compounds wherein Z is substituted chroman-2-yl, 2,3-dihydrobenzofuran-2-yl, etc. have an effect of inhibiting the formation of lipid peroxides too.

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