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2-(Chloromethyl)-4-fluoro-1-methoxybenzene, a benzene derivative with the molecular formula C8H8ClFO, features a chlorine and fluorine atom attached to the benzene ring, along with a methoxy group. This chemical compound is utilized in organic synthesis and chemical reactions, and it holds potential in the pharmaceutical industry as a precursor for the synthesis of various drugs and pharmaceuticals. Due to its potential hazardous properties, it is crucial to handle and store 2-(CHLOROMETHYL)-4-FLUORO-1-METHOXYBENZENE with caution, ensuring that only trained professionals work with it in a controlled laboratory environment.

19415-40-8

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19415-40-8 Usage

Uses

Used in Organic Synthesis:
2-(Chloromethyl)-4-fluoro-1-methoxybenzene is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure, with a chloromethyl group, allows for further functionalization and the creation of a wide range of derivatives.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(Chloromethyl)-4-fluoro-1-methoxybenzene is used as a building block for the synthesis of drugs and pharmaceuticals. Its presence in the molecular structure can contribute to the development of new therapeutic agents with specific properties, such as improved pharmacokinetics or targeted delivery.
Used in Chemical Reactions:
2-(Chloromethyl)-4-fluoro-1-methoxybenzene is employed as a reactant in various chemical reactions, where its functional groups can participate in substitution, addition, or other types of reactions to yield desired products. Its versatility in chemical transformations makes it a valuable compound in the field of chemistry.
Used in Research and Development:
2-(Chloromethyl)-4-fluoro-1-methoxybenzene is utilized in research and development for the exploration of new chemical pathways and the discovery of novel compounds with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 19415-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,1 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19415-40:
(7*1)+(6*9)+(5*4)+(4*1)+(3*5)+(2*4)+(1*0)=108
108 % 10 = 8
So 19415-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClFO/c1-11-8-3-2-7(10)4-6(8)5-9/h2-4H,5H2,1H3

19415-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(chloromethyl)-4-fluoro-1-methoxybenzene

1.2 Other means of identification

Product number -
Other names 2-chloromethyl-4-fluoro-1-methoxy-benzene

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:19415-40-8 SDS

19415-40-8Relevant academic research and scientific papers

PHENOXYACETIC ACID DERIVATIVES USEFUL FOR TREATING RESPIRATORY DISEASES

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Page/Page column 76-77, (2008/06/13)

The invention relates to substituted phenoxyacetic acids as useful pharmaceutical compounds for treating respiratory disorders, pharmaceutical compositions containing them, and processes for their preparation.Formula (I)

NOVEL DERIVATIVES OF DICARBOXYLIC ACID HAVING PHARMACEUTICAL PROPERTIES

-

Page/Page column 39-40, (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; 127, (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 129-130, (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.

MORPHOLINE DERIVATIVES AS NOREPINEPHRINE REUPTAKE INHIBITORS

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Page/Page column 52-53, (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.

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

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Page/Page column 132-133; 278, (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.

ARYL AND HETEROARYL MORPHOLINE DERIVATIVES

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Page 22-23, (2008/06/13)

Compounds of formula (I) are selective inhibitors of the reuptake of norepinephrine, wherein Rx is H; Ry is H or C1-C4 alkyl; each Rz is independently H or C1-C4 alkyl; X represents O; Y represents OH or OR; R is C1-C4 alkyl; and Ar1 and Ar2 are optionall

Stereoselectivity and Generality of the Palladium-Catalysed Cyclopropanation of α,β-Unsaturated Carboxylic Acids Derivatized with Oppolzer's Sultam

Vallaerda, Jerk,Appelberg, Ulf,Csoeregh, Ingeborg,Hacksell, Uli

, p. 461 - 470 (2007/10/02)

A series of α,β-unsaturated carboxylic acids derivatized with camphorsultam 1 a s a chiral auxiliary has been stereoselectively cyclopropanated. the selectivity of the reaction produces cyclopropanated products with the 1R,2R absolute configuration as indicated by the optical rotations as well as by an X-ray structure determineation.The temperature dependence of the reaction was studied with three substrates. the highest stereoselectivity was obtained at temperatures above 25 deg C.Branching at the α- or β-carbons disfavours complete conversion, and electron-withdrawing substituents at these positions seem to prevent the reaction.The auxiliary was removed by using titanium(IV) isopropoxide in benzyl alcohol followed by alkaline hydrolysis of the intermediate ester. the potent 5-HT1A receptor agonist (1R,2S)-2-(2-hydroxyphenyl)-N,N-dipropylcyclopropylamine 13 was synthesized by this method

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