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62558-08-1

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62558-08-1 Usage

General Description

[5-fluoro-2-(hydroxymethyl)phenyl]methanol, also known as fluoromethol, is a chemical compound with the molecular formula C8H9FO2. It is a derivative of phenylmethanol, containing a fluorine atom at the 5 position and a hydroxymethyl group at the 2 position of the phenyl ring. [5-fluoro-2-(hydroxymethyl)phenyl]methanol is commonly used in the synthesis of pharmaceuticals and organic compounds. It is known for its mildew-inhibiting properties and is used as an intermediate in the production of various pharmaceuticals and agrochemicals. Fluoromethol is also used as a building block in the synthesis of various biologically active compounds due to its unique structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 62558-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,5 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62558-08:
(7*6)+(6*2)+(5*5)+(4*5)+(3*8)+(2*0)+(1*8)=131
131 % 10 = 1
So 62558-08-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9FO2/c9-8-2-1-6(4-10)7(3-8)5-11/h1-3,10-11H,4-5H2

62558-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-fluoro-2-(hydroxymethyl)phenyl]methanol

1.2 Other means of identification

Product number -
Other names 4-Fluoro-1,2-Benzenedimethanol

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:62558-08-1 SDS

62558-08-1Relevant articles and documents

IDO/TDO Inhibitor

-

Paragraph 0334-0336, (2020/08/19)

A compound of formula (I) given below or a pharmaceutically acceptable salt of the compound is useful as an IDO/TDO inhibitor. Thus, the compound of formula (I) or the pharmaceutically acceptable salt of the compound can be used as, for example, a therapeutic agent for a disease or a disorder selected from tumor, infectious disease, neurodegenerative disorder, cataract, organ transplant rejection, autoimmune disease, postoperative cognitive impairment, and disease related to women's reproductive health [in the following formula (I), ring A represents an aromatic ring, an aliphatic ring, a heterocyclic ring, or a condensed ring of two or more rings selected from an aromatic ring, an aliphatic ring and a heterocyclic ring; X, R1 and R2 represent a substituent on a ring atom constituting ring A; m represents an integer of 0 to 6; X represents, for example, a halogen atom; and R1 and R2 are the same or different and are selected from, for example, the group consisting of groups of formula (a) or formula (b); and in the following formula (a) and formula (b), Y is selected from the group consisting of O, S, and Se, Z is selected from the group consisting of O, S, and Se, n represents an integer of 1 to 8, r represents an integer of 1 to 8, s represents an integer of 1 to 8, R4 represents, for example, —C(═NH)—HN2, and R6 represents, for example, a substituted or unsubstituted aryl group].

FlICk (fluorescent isoindole crosslinking) for peptide stapling

Todorovic, Mihajlo,Perrin, David M.

, p. 313 - 332 (2020/05/18)

The rigidification of peptide secondary structure via stapling is an important and enduring goal in the development of functional peptides for biochemical and pharmaceutical applications. In addition, the incorporation of fluorophores and chromophores has

Platinum-on-Carbon-Catalyzed Aqueous Oxidative Lactonization of Diols by Using Molecular Oxygen

Ban, Kazuho,Sajiki, Hironao,Sawama, Yoshinari,Takakura, Ryoya

supporting information, p. 1919 - 1923 (2019/09/30)

A lactonization of various diols catalyzed by platinum on carbon (Pt/C) in water under an atmosphere of molecular oxygen was developed. Derivatives of 1,4- 1,5- and 1,6-diols were transformed into the corresponding five-, six-, and seven-membered lactones by the present oxidative lactonization method.

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