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CAS

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300355-23-1

4-chloro-3-nitrophenylacetic acid methyl ester is a chemical compound characterized by the presence of a methyl ester group attached to a 4-chloro-3-nitrophenylacetic acid molecule. It is a yellow crystalline solid with the chemical formula C9H8ClNO5. 4-chloro-3-nitrophenylacetic acid methyl ester is known for its utility in the synthesis of pharmaceutical and agrochemical products, as well as its role in organic synthesis and chemical research. The 4-chloro and 3-nitro groups in its structure contribute to its versatility as a building block for the preparation of various functionalized organic compounds.

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  • 300355-23-1 Structure

  • Basic information

    1. Product Name: 4-chloro-3-nitrophenylacetic acid methyl ester
    2. Synonyms: 4-chloro-3-nitrophenylacetic acid methyl ester
    3. CAS NO:300355-23-1
    4. Molecular Formula:
    5. Molecular Weight: 229.62
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 300355-23-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 336.0±27.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.382±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-chloro-3-nitrophenylacetic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-chloro-3-nitrophenylacetic acid methyl ester(300355-23-1)
    11. EPA Substance Registry System: 4-chloro-3-nitrophenylacetic acid methyl ester(300355-23-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 300355-23-1(Hazardous Substances Data)

300355-23-1 Usage

Uses

Used in Pharmaceutical Synthesis:
4-chloro-3-nitrophenylacetic acid methyl ester is used as an intermediate in the synthesis of pharmaceutical products for its ability to be incorporated into the molecular structures of various drugs. Its presence in the molecule allows for the creation of new compounds with potential therapeutic properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4-chloro-3-nitrophenylacetic acid methyl ester is utilized as an intermediate in the production of agrochemicals, such as pesticides and herbicides. Its unique structure enables the development of compounds that can effectively control pests and weeds in agricultural settings.
Used in Organic Synthesis:
4-chloro-3-nitrophenylacetic acid methyl ester is employed as a reagent in organic synthesis, where it can be used to form a variety of organic compounds. Its functional groups facilitate reactions that lead to the formation of new molecules with different properties and applications.
Used in Chemical Research:
As a reagent in chemical research, 4-chloro-3-nitrophenylacetic acid methyl ester is used to study various chemical reactions and mechanisms. Its presence in the molecule allows researchers to explore its reactivity and potential applications in the development of new chemical processes and compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 300355-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,0,3,5 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 300355-23:
(8*3)+(7*0)+(6*0)+(5*3)+(4*5)+(3*5)+(2*2)+(1*3)=81
81 % 10 = 1
So 300355-23-1 is a valid CAS Registry Number.

300355-23-1Relevant articles and documents

Discovery of piragliatin-first glucokinase activator studied in type 2 diabetic patients

Sarabu, Ramakanth,Bizzarro, Fred T.,Corbett, Wendy L.,Dvorozniak, Mark T.,Geng, Wanping,Grippo, Joseph F.,Haynes, Nancy-Ellen,Hutchings, Stanley,Garofalo, Lisa,Guertin, Kevin R.,Hilliard, Darryl W.,Kabat, Marek,Kester, Robert F.,Ka, Wang,Liang, Zhenmin,Mahaney, Paige E.,Marcus, Linda,Matschinsky, Franz M.,Moore, David,Racha, Jagdish,Radinov, Roumen,Ren, Yi,Qi, Lida,Pignatello, Michael,Spence, Cheryl L.,Steele, Thomas,Tengi, John,Grimsby, Joseph

supporting information, p. 7021 - 7036 (2012/11/07)

Glucokinase (GK) activation as a potential strategy to treat type 2 diabetes (T2D) is well recognized. Compound 1, a glucokinase activator (GKA) lead that we have previously disclosed, caused reversible hepatic lipidosis in repeat-dose toxicology studies.

Tetrahydrocarbazol derivatives as ligands for G-protein-coupled receptors (GPCR)

-

Page 13 - 14, (2010/11/30)

This invention provides new tetrahydrocarbazole derivatives that act as ligands for G-protein-coupled receptors (GPCR), especially as antagonists of the gonadotropin-releasing hormone (GnRH). A pharmaceutical composition that contains these new tetrahydro

Fused heteroaromatic glucokinase activators

-

, (2008/06/13)

Glucokinase activating amides are useful for increasing insulin secretion in the treatment of type II diabetes.

Heteroaromatic glucokinase activators

-

, (2008/06/13)

2,3-Di-substituted N-heteroaromatic propionamides with said substitution at the 2-position being a substituted phenyl group and at the 3-position being a cycloalkyl ring, said propionamides being glucokinase activators which increase insulin secretion in the treatment of type II diabetes.

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