3094-25-5 Usage
Description
1-(ChloroMethyl)-4-fluoronaphthalene is a chemical compound with the molecular formula C11H8ClF. It is a derivative of naphthalene, featuring a chloromethyl group and a fluorine atom. This colorless to light yellow liquid with a strong odor is known for its moderate toxicity, necessitating careful handling and storage to prevent potential hazards.
Uses
Used in Pharmaceutical Industry:
1-(ChloroMethyl)-4-fluoronaphthalene is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Dye Industry:
In the dye industry, 1-(ChloroMethyl)-4-fluoronaphthalene is utilized as an intermediate for the production of dyes, where its unique chemical structure aids in creating dyes with desired color characteristics.
Used in Agrochemical Industry:
1-(ChloroMethyl)-4-fluoronaphthalene is employed as a starting material in the synthesis of agrochemicals, contributing to the development of effective compounds for agricultural applications.
Used in Fluorinated Compounds Production:
As a precursor, 1-(ChloroMethyl)-4-fluoronaphthalene is used in the production of other fluorinated compounds, highlighting its versatility in various chemical reactions and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3094-25-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,9 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3094-25:
(6*3)+(5*0)+(4*9)+(3*4)+(2*2)+(1*5)=75
75 % 10 = 5
So 3094-25-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H8ClF/c12-7-8-5-6-11(13)10-4-2-1-3-9(8)10/h1-6H,7H2
3094-25-5Relevant articles and documents
Pd-catalyzed allylative dearomatisation using Grignard reagents
Boldrini, Cosimo,Harutyunyan, Syuzanna R.
, p. 11807 - 11810 (2021/11/30)
Pd-catalyzed allylative dearomatisation of naphthyl halides is shown to be feasible by employing Grignard reagents. The high reactivity of the nucleophile allows for fast reactions and low catalyst loading, while a plethora of successfully substituted compounds illustrate the broad scope. Five membered heteroaromatic compounds are also demonstrated to be reactive under similar conditions.
