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Benzenemethanol, 5-fluoro-2-methoxy(9CI) is a highly specific organic compound distinguished by its benzene ring structure with a unique substitution pattern. The benzene ring, a six-carbon ring with alternating single and double bonds, is attached to a methanol unit. Benzenemethanol, 5-fluoro-2-methoxy(9CI) is further characterized by the presence of a fluorine atom at the 5th position and a methoxy group at the 2nd position, which significantly influence its chemical and physical properties, including its reactivity. This distinctive structure makes it a versatile compound with potential applications across various industries.

426831-32-5

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426831-32-5 Usage

Uses

Used in Pharmaceutical Industry:
Benzenemethanol, 5-fluoro-2-methoxy(9CI) is used as a reactant in pharmaceutical synthesization for the development of new drugs. Its unique structure and reactivity make it a promising candidate for the creation of complex organic compounds with potential therapeutic applications.
Used in Chemical Synthesis:
In the chemical industry, Benzenemethanol, 5-fluoro-2-methoxy(9CI) serves as a key reactant in the synthesis of other complex organic compounds. Its specific functional groups and reactivity allow for the formation of a wide range of chemical products, contributing to the advancement of various chemical processes.
Used in Research and Development:
Benzenemethanol, 5-fluoro-2-methoxy(9CI) is utilized in research and development settings to explore its chemical properties and potential applications. Further studies are needed to confirm and clarify its uses, particularly in the pharmaceutical and chemical synthesis industries, where its unique structure and reactivity could offer significant advantages.

Check Digit Verification of cas no

The CAS Registry Mumber 426831-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,6,8,3 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 426831-32:
(8*4)+(7*2)+(6*6)+(5*8)+(4*3)+(3*1)+(2*3)+(1*2)=145
145 % 10 = 5
So 426831-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H9FO2/c1-11-8-3-2-7(9)4-6(8)5-10/h2-4,10H,5H2,1H3

426831-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-Fluoro-2-methoxyphenyl)methanol

1.2 Other means of identification

Product number -
Other names (5-fluoro-2-methoxyphenyl)methanol

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:426831-32-5 SDS

426831-32-5Relevant articles and documents

Synthesis of Phenanthridines through Palladium-Catalyzed Cascade Reaction of 2-Halo-N-Ms-arylamines with Benzyl Halides/Sulfonates

Yang, Si-Yi,Han, Wen-Yong,Zhang, Ding-Lei,Zhou, Xiao-Jian,Bai, Mei,Cui, Bao-Dong,Wan, Nan-Wei,Yuan, Wei-Cheng,Chen, Yong-Zheng

, p. 996 - 1003 (2017/02/15)

An efficient palladium-catalyzed nucleophilic substitution/C–H activation/aromatization cascade reaction between readily available 2-halo-N-Ms-arylamines (Ms = methanesulfonyl) and benzyl halides/sulfonates has been described. A wide variety of phenanthridines were synthesized in a one-pot fashion in moderate to high yields (37–86 %). Notably, this method provides a straightforward, facile approach for the synthesis of phenanthridines. The practicality was further substantiated by successfully carrying out a gram-scale preparation.

Telescoped approach to aryl hydroxymethylation in the synthesis of a key pharmaceutical intermediate

Slattery, Catherine N.,Deasy, Rebecca E.,Maguire, Anita R.,Kopach, Michael E.,Singh, Utpal K.,Argentine, Mark D.,Trankle, William G.,Scherer, Roger Brian,Moynihan, Humphrey

, p. 5955 - 5963 (2013/07/26)

An efficient synthetic approach leading to introduction of the hydroxymethyl group to an aryl moiety via combination of the Bouveault formylation and hydride reduction has been optimized using a rational, mechanistic-based approach. This approach enabled

SUBSTITUTED PIPERIDINES THAT INCREASE p53 ACTIVITY AND THE USES THEREOF

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Page/Page column 148, (2011/05/05)

The present invention provides a compound of Formula (1) as described herein or a pharmaceutically acceptable salt, solvate or ester thereof. The compounds are useful as inhibitors of the HDM2 protein. Also disclosed are pharmaceutical compositions comprising the above compounds and methods of treating cancer using the same.

CHROMANE AND CHROMENE DERIVATIVES AND USES THEREOF

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Page/Page column 73-74, (2010/11/28)

Methods of preparing compounds of formula (I) or pharmaceutically acceptable salts thereof are provided wherein each of R1, R2, R3, R4, x, m, n, and Ar are as defined, and described in classes and subclasses herein, which are agonists or partial agonists of the 2C subtype of brain serotonin receptors. The compounds, and compositions containing the compounds, can be used to treat a variety of central nervous system disorders such as schizophrenia.

ORGANIC COMPOUNDS

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Page/Page column 21, (2008/06/13)

A compound of formula (I); in free or pharmaceutically acceptable salt form, where R1, R2, R3, R4, R5, m, n, w, X, Y and Q have the meanings as indicated in the specification, are useful for treating conditions mediated by the CRTh2 receptor, especially inflammatory or obstructive airways diseases.

NOVEL DERIVATIVES OF DICARBOXYLIC ACID HAVING PHARMACEUTICAL PROPERTIES

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Page/Page column 39, (2008/06/13)

The invention relates to compounds of formulae (II), (IV), and (VI) as shown below, wherein the several variable groups are as defined in the specification and claims. Processes for making these materials, and methods for using them in the synthesis of compounds for treatment of cardiovascular disorders and fibrotic disorders are also disclosed.

TREATMENT OF LEARNING DISABILITIES AND MOTOR SKILLS DISORDER WITH NOREPINEPHRINE REUPTAKE INHIBITORS

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Page/Page column 126, (2010/02/11)

Provided are methods and medicaments for treating a learning disability or a Motor Skills Disorder, comprising administering to a patient in need of such treatment an effective amount of a selective norepinephrine reuptake inhibitor.

TREATMENT OF PERVASIVE DEVELOPMENTAL DISORDERS WITH NOREPINEPHRINE REUPTAKE INHIBITORS

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Page/Page column 129, (2010/02/11)

Provided are methods and medicaments for treating a Pervasive Developmental Disorder, comprising administering to a patient in need of such treatment an effective amount of a selective norepinephrine reuptake inhibitor.

TREATMENT OF HOT FLASHES, IMPULSE CONTROL DISORDERS AND PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION

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Page/Page column 132; 277, (2010/02/12)

Selective norepinephrine reuptake inhibitors are useful for the prevention or treatment of hot flashes, vasomotor symptoms, impulse control disorders or personality change due to a general medical condition.

MORPHOLINE DERIVATIVES AS NOREPINEPHRINE REUPTAKE INHIBITORS

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Page/Page column 52, (2010/02/11)

Compounds of the general formula (I) are inhibitors of the reuptake of norepinephrine. As such, they may be useful for the treatment of disorders of the central and/or peripheral nervous system.

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