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1-(2,2-diphenylethyl)-2-fluorobenzene is an organic compound with the molecular formula C25H21F. It is a derivative of benzene, featuring a fluorine atom at the 2-position and a 2,2-diphenylethyl group attached to the 1-position. This molecule is characterized by its unique structure, which consists of a benzene ring with a fluorine atom and a bulky diphenylethyl side chain. The presence of the fluorine atom and the diphenylethyl group imparts specific chemical and physical properties to the compound, making it potentially useful in various applications, such as in the synthesis of pharmaceuticals or as a building block in organic chemistry. The compound's structure also suggests that it may have unique electronic properties due to the influence of the fluorine atom on the aromatic system.

1229-66-9

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1229-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1229-66-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1229-66:
(6*1)+(5*2)+(4*2)+(3*9)+(2*6)+(1*6)=69
69 % 10 = 9
So 1229-66-9 is a valid CAS Registry Number.

1229-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,2-diphenylethyl)-2-fluorobenzene

1.2 Other means of identification

Product number -
Other names 1,1-Diphenyl-2-(o-fluorophenyl)ethane

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 -
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More Details:1229-66-9 SDS

1229-66-9Upstream product

1229-66-9Downstream Products

1229-66-9Relevant academic research and scientific papers

Formation of 2-arylnaphthalenes from N-tosylated phenylalanine derivatives

Seong, Mi Ra,Song, Hyun Nam,Kim, Jae Nyoung

, p. 7101 - 7104 (1998)

N-Tosylated phenylalanine derivatives in benzene in the presence of sulfuric acid afforded 2-arylnaphthalene derivatives in moderate yields. The reaction might proceed via the corresponding decarbonylated N-tosylimine derivatives. Aldol type reaction of N-tosylimines followed by intramolecular Friedel-Crafts reaction and elimination of p-toluenesulfonamide gave 2- arylnaphthalenes.

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