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104173-41-3

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104173-41-3 Usage

General Description

1-[3-(trifluoromethyl)phenyl]cyclopropane-1-carboxylic acid is a chemical compound with a molecular formula C12H11F3O2. It is a cyclopropane carboxylic acid derivative that contains a trifluoromethylphenyl group. 1-[3-(trifluoromethyl)phenyl]cyclopropane-1-carboxylic acid has been studied for its potential use as a building block in the synthesis of pharmaceuticals and agrochemicals. It exhibits a unique structure and reactivity due to the presence of the cyclopropane and trifluoromethyl moieties, which makes it an interesting target for chemical research and development. Additionally, the presence of the carboxylic acid group suggests potential applications in medicinal chemistry as a potential drug candidate.

Check Digit Verification of cas no

The CAS Registry Mumber 104173-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,7 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104173-41:
(8*1)+(7*0)+(6*4)+(5*1)+(4*7)+(3*3)+(2*4)+(1*1)=83
83 % 10 = 3
So 104173-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H9F3O2/c12-11(13,14)8-3-1-2-7(6-8)10(4-5-10)9(15)16/h1-3,6H,4-5H2,(H,15,16)

104173-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(trifluoromethyl)phenyl]cyclopropane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-[3-(Trifluoromethyl)phenyl]cyclopropanecarboxylic acid

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:104173-41-3 SDS

104173-41-3Relevant articles and documents

Rhodium-Catalyzed Enantioselective Silylation of Cyclopropyl C?H Bonds

Lee, Taegyo,Hartwig, John F.

, p. 8723 - 8727 (2016/07/21)

Hydrosilyl ethers, generated in situ by the dehydrogenative silylation of cyclopropylmethanols with diethylsilane, undergo asymmetric, intramolecular silylation of cyclopropyl C?H bonds in high yields and with high enantiomeric excesses in the presence of

Methods and Compositions for Selectin Inhibition

-

Page/Page column 19-20, (2008/12/04)

The present teachings relate to novel compounds of formula I: wherein the constituent variables are as defined herein. Compounds of the present teachings can act as antagonists of the mammalian adhesion proteins known as selecting. Methods for treating or preventing selectin-mediated disorders are provided, which include administration of these compounds in a therapeutically effective amount.

Deamination Reactions, 45. Decomposition of 1-Arylcyclopropanediazonium Ions

Kirmse, Wolfgang,Rode, Jutta

, p. 3694 - 3703 (2007/10/02)

1-Arylcyclopropanediazonium ions have been generated by alkaline cleavage of the analogous nitrosocarbamates in methanol.With increasing ?-donor capacity of the aryl groups, retention of the three-membered ring was enhanced while the stereoselectivity (as probed with the aid of 2-D labels) was diminished or entirely lost (4-methoxyphenyl).Where applicable, the stereoselectivity of ring opening is inferior to that of nucleophilic displacement.The data may be interpreted in terms of competing reactions (ks, kc, kΔ) of the cyclopropanediazonium ions.

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