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Phenyl, 2-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52009-05-9

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52009-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52009-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,0 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52009-05:
(7*5)+(6*2)+(5*0)+(4*0)+(3*9)+(2*0)+(1*5)=79
79 % 10 = 9
So 52009-05-9 is a valid CAS Registry Number.

52009-05-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxyphenyl radical

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:52009-05-9 SDS

52009-05-9Downstream Products

52009-05-9Relevant academic research and scientific papers

Compounds for and methods of treating diseases

-

, (2021/10/27)

The present invention provides heterocyclic compounds of formula (I) that modulate biological metals and to pharmaceutical compositions containing such compounds. The invention particularly relates to compounds that modulate iron and to compounds for the treatment of diseases, particularly neurological diseases such as Parkinson's disease (PD), Alzheimer's disease (AD), Alzheimer-type dementia, Huntington's disease (HD), amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD) and multiple system atrophy (MSA).

Structure and infrared spectrum of 2-hydroxyphenyl radical

Nagata, Mitsuhiro,Futami, Yoshisuke,Akai, Nobuyuki,Kudoh, Satoshi,Nakata, Munetaka

, p. 259 - 264 (2007/10/03)

Infrared spectrum of 2-hydroxyphenyl, ·C 6H4-OH, produced from 2-iodophenol in a low-temperature argon matrix upon UV irradiation (λ>280 nm) was measured with an FT-IR spectrophotometer. This radical was found to be less stable by 120 kJ mol -1 than phenoxyl, C6H5-O·, by a density functional theory calculation. Two final photoproducts were identified as cyclopentadienylidenemethanone and 4-iodo-2,5-cyclohexadienone in analogy with the photoproducts of 2-chloro and 2-bromophenols. A kinetic analysis shows that the latter is produced via 2-hydroxyphenyl by hydrogen migration and iodine recombination while the former is produced by Wolff rearrangement after elimination of hydrogen iodide.

Thermal properties of 1,1′-bis(p-substituted-benzoyloxy-substituted-phenyl)cyclohexanes

Rajkotia,Parsania

, p. 24 - 27 (2007/10/03)

DSC thermograms of 1,1′-bis(p-substituted-benzoyloxy-substituted-phenyl)cyclohexanes 3, 8, 14 and 15 showed two endotherms whereas 2, 4-7, 9, 11-13, 16 and 17 showed more than two endotherms indicating formation of new compounds as a result of decomposition of original compound. TG thermograms of 1, 2, 4, 5, 8, 11-13 and 15 involved a single step decomposition whereas 3, 6, 7, 9, 10, 14, 16 and 17 involved two step degradation and involved first order kinetics.

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