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2-Ethyl-3-methyl-2-(propan-2-yl)butanoic acid is a complex organic compound with the molecular formula C10H20O2. It is a carboxylic acid, characterized by the presence of a carboxyl group (-COOH). The structure of 2-ethyl-3-methyl-2-(propan-2-yl)butanoic acid features a butanoic acid chain with various alkyl groups attached to it. Specifically, it has an ethyl group (C2H5) at the 2nd carbon, a methyl group (CH3) at the 3rd carbon, and a propyl group (C3H7) at the 2nd carbon, with the propyl group being a secondary (2-) isomer. 2-ethyl-3-methyl-2-(propan-2-yl)butanoic acid is an isomer of valproic acid, a medication used to treat certain types of epilepsy and bipolar disorder. Due to its complex structure, 2-ethyl-3-methyl-2-(propan-2-yl)butanoic acid may have unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research.

7498-50-2

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7498-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7498-50-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7498-50:
(6*7)+(5*4)+(4*9)+(3*8)+(2*5)+(1*0)=132
132 % 10 = 2
So 7498-50-2 is a valid CAS Registry Number.

7498-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-3-methyl-2-propan-2-ylbutanoic acid

1.2 Other means of identification

Product number -
Other names 2,2-Diisopropyl-buttersaeure

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:7498-50-2 SDS

7498-50-2Downstream Products

7498-50-2Relevant academic research and scientific papers

Rh-catalyzed intermolecular reactions of cyclic α-diazocarbonyl compounds with selectivity over tertiary C-H bond migration

Deangelis, Andrew,Dmitrenko, Olga,Fox, Joseph M.

supporting information; experimental part, p. 11035 - 11043 (2012/08/28)

Intermolecular Rh-catalyzed reactions of cyclic α-diazocarbonyl compounds with chemoselectivity over β-hydride elimination are described. These methods represent the first general intermolecular reactions of Rh-carbenoids that are selective over tertiary

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