Welcome to LookChem.com Sign In|Join Free

CAS

  • or

26073-09-6

Post Buying Request

26073-09-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

26073-09-6 Usage

General Description

Ethyl 4-methyl-2-oxovalerate, also known as ethyl isohexanoate, is a chemical compound with the molecular formula C7H12O3. It is an ester, which is a type of organic compound formed by the reaction of an alcohol with a carboxylic acid. Ethyl 4-methyl-2-oxovalerate has a fruity, sweet odor and is commonly used as a flavoring agent in the food and beverage industry. It is also used in the production of perfumes and fragrances due to its pleasant scent. Additionally, this chemical is sometimes used as a solvent or as an intermediate in the synthesis of other organic compounds. Ethyl 4-methyl-2-oxovalerate is considered to be relatively safe and is approved for use in food products by regulatory agencies such as the US Food and Drug Administration.

Check Digit Verification of cas no

The CAS Registry Mumber 26073-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,7 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26073-09:
(7*2)+(6*6)+(5*0)+(4*7)+(3*3)+(2*0)+(1*9)=96
96 % 10 = 6
So 26073-09-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O3/c1-4-11-8(10)7(9)5-6(2)3/h6H,4-5H2,1-3H3

26073-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methyl-2-oxo-pentanoic acid ethyl ester

1.2 Other means of identification

Product number -
Other names -

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:26073-09-6 SDS

26073-09-6Relevant articles and documents

Dinaphthoporphycenes

Roznyatovskiy, Vladimir,Lynch, Vincent,Sessler, Jonathan L.

, p. 4424 - 4427 (2010)

Figure Presented. Naphthobipyrrole is a potentially useful building block for porphyrin and porphyrin analogue synthesis. Reported here is a simple, generalizable synthetic route to α-formylated, β-substituted naphthobipyrroles and their use in the preparation of binaphthoporphycenes. The resulting binaphthoporphycenes possess a planar geometry as determined via a single-crystal X-ray diffraction analysis; they also display absorption maxima that are bathochromically shifted compared to simple porphycenes.

Design, synthesis and antimalarial evaluation of novel thiazole derivatives

Bueno, José María,Carda, Miguel,Crespo, Benigno,Cu?at, Ana Carmen,de Cozar, Cristina,León, María Luisa,Marco, J. Alberto,Roda, Nuria,Sanz-Cervera, Juan F.

supporting information, p. 3938 - 3944 (2016/08/01)

As part of our medicinal chemistry program's ongoing search for compounds with antimalarial activity, we prepared a series of thiazole analogs and conducted a SAR study analyzing their in vitro activities against the chloroquine-sensitive Plasmodium falciparum 3D7 strain. The results indicate that modifications of the N-aryl amide group linked to the thiazole ring are the most significant in terms of in vitro antimalarial activity, leading to compounds with high antimalarial potency and low cytotoxicity in HepG2 cell lines. Furthermore, the observed SAR implies that non-bulky, electron-withdrawing groups are preferred at ortho position on the phenyl ring, whereas small atoms such as H or F are preferred at para position. Finally, replacement of the phenyl ring by a pyridine affords a compound with similar potency, but with potentially better physicochemical properties which could constitute a new line of research for further studies.

3-substituted indole antiproliferative angiogenesis inhibitors

-

, (2008/06/13)

3-Substituted indole carbohydrazides having the formula are useful for inhibiting angiogenesis and cell proliferation. Also disclosed are compositions which inhibit angiogenesis and cell proliferation and methods of inhibiting angiogenesis and cancer in a mammal.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 26073-09-6