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2924-25-6

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2924-25-6 Usage

General Description

1-(1-propenyl)-3-(trifluoromethyl)benzene is a chemical compound with the molecular formula C10H9F3. It is a colorless liquid with a sweet, fruity odor and is commonly used as a flavoring agent in the food and beverage industry. 1-(1-propenyl)-3-(trifluoromethyl)benzene is also used in the production of synthetic fragrances and as a chemical intermediate in the manufacturing of pharmaceuticals and agrochemicals. It is important to handle this compound carefully due to its potential health hazards, including respiratory and skin irritation. Additionally, 1-(1-propenyl)-3-(trifluoromethyl)benzene is not known to be persistent in the environment and is not expected to bioaccumulate.

Check Digit Verification of cas no

The CAS Registry Mumber 2924-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2924-25:
(6*2)+(5*9)+(4*2)+(3*4)+(2*2)+(1*5)=86
86 % 10 = 6
So 2924-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H9F3/c1-2-4-8-5-3-6-9(7-8)10(11,12)13/h2-7H,1H3/b4-2+

2924-25-6SDS

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 1-(1-propenyl)-3-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 1-propenyl-3-trifluoromethyl-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:2924-25-6 SDS

2924-25-6Downstream Products

2924-25-6Relevant articles and documents

Nickel-catalyzed direct electrochemical cross-coupling between aryl halides and activated alkyl halides

Durandetti, Muriel,Nedelec, Jean-Yves,Perichon, Jacques

, p. 1748 - 1755 (2007/10/03)

The electrochemical reduction of a mixture of aryl halides and activated alkyl halides in DMF in the presence of catalytic amount of NiBr2bipy leads to cross-coupling products in good to high yields. The method applies to the synthesis of α-aryl ketones, α-aryl esters, and allylated compounds from readily available organic halides. Optimization of the process has been obtained by slowly adding the most reactive organic halide (usually the activated alkyl halide) during the electrolysis which is best conducted at 70 °C when aryl bromides are involved.

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