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601-75-2

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601-75-2 Usage

Description

Ethylmalonic acid is an important organic intermediate with a versatile chemical structure that allows it to be utilized in various applications across different industries.

Uses

Used in Agrochemical Industry:
Ethylmalonic acid is used as a key intermediate for the synthesis of various agrochemicals, such as pesticides and herbicides, due to its ability to form stable and effective compounds that can protect crops from pests and diseases.
Used in Pharmaceutical Industry:
Ethylmalonic acid serves as a crucial building block in the development of pharmaceutical compounds, contributing to the creation of drugs with specific therapeutic properties. Its unique structure allows for the design of molecules that can target and treat a wide range of medical conditions.
Used in Dye Industry:
Ethylmalonic acid is used as a vital component in the production of dyes, particularly in the synthesis of colorants for various applications. Its chemical properties enable the creation of dyes with desirable characteristics, such as color intensity, stability, and resistance to fading.

Check Digit Verification of cas no

The CAS Registry Mumber 601-75-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 601-75:
(5*6)+(4*0)+(3*1)+(2*7)+(1*5)=52
52 % 10 = 2
So 601-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O4/c1-2-3(4(6)7)5(8)9/h3H,2H2,1H3,(H,6,7)(H,8,9)/p-2

601-75-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B20715)  Ethylmalonic acid, 98%   

  • 601-75-2

  • 5g

  • 347.0CNY

  • Detail
  • Alfa Aesar

  • (B20715)  Ethylmalonic acid, 98%   

  • 601-75-2

  • 25g

  • 1458.0CNY

  • Detail
  • Alfa Aesar

  • (B20715)  Ethylmalonic acid, 98%   

  • 601-75-2

  • 100g

  • 5191.0CNY

  • Detail
  • Aldrich

  • (102687)  Ethylmalonicacid  97%

  • 601-75-2

  • 102687-5G

  • 436.41CNY

  • Detail
  • Aldrich

  • (102687)  Ethylmalonicacid  97%

  • 601-75-2

  • 102687-50G

  • 2,875.86CNY

  • Detail

601-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethylmalonic acid

1.2 Other means of identification

Product number -
Other names Propanedioic acid, ethyl-

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:601-75-2 SDS

601-75-2Relevant articles and documents

Synthesis of Cyclopentenones through Rhodium-Catalyzed C-H Annulation of Acrylic Acids with Formaldehyde and Malonates

Yu, Shuling,Hong, Chao,Liu, Zhanxiang,Zhang, Yuhong

supporting information, p. 5054 - 5059 (2021/07/20)

An efficient rhodium-catalyzed protocol for the synthesis of cyclopentenones based on a three-component reaction of acrylic acids, formaldehyde, and malonates via vinylic C-H activation is reported. Exploratory studies showed that 5-alkylation of as-prepared cyclopentenones could be realized smoothly by the treatment of a variety of alkyl halides with a Na2CO3/MeOH solution. Excess formaldehyde and malonate led to a multicomponent reaction that afforded the multisubstituted cyclopentenones through a Michael addition.

SULFONYL-SUBSTITUTED BICYCLIC COMPOUND WHICH ACTS AS ROR INHIBITOR

-

Paragraph 0325; 0326, (2020/08/16)

Provided is a sulfonyl-substituted bicyclic compound (A) which acts as a RORγ inhibitor, said compound has good RORγ inhibitory activity and is expected to be used for treating diseases mediated by a RORγ receptor in mammals.

Copper-catalyzed intermolecular chloro- and bromotrifluoromethylation of alkenes

Fu, Mingyang,Chen, Long,Jiang, Yongpeng,Jiang, Zhong-Xing,Yang, Zhigang

supporting information, p. 348 - 351 (2016/02/19)

A highly practical copper-catalyzed intermolecular halotrifluoromethylation of alkenes has been developed under mild reaction conditions. A variety of Cl/Br-containing trifluoromethyl derivatives were directly synthesized from a wide range of alkenes, including electron-deficient and unactivated alkenes.

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