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(4-ETHOXY-3-NITROPHENYL)ACETIC ACID, with the molecular formula C10H10NO5, is a chemical compound derived from acetic acid. It features a nitro group and an ethoxy group attached to a phenyl ring, making it a versatile compound with potential applications across various fields.

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  • 373361-54-7 Structure
  • Basic information

    1. Product Name: (4-ETHOXY-3-NITROPHENYL)ACETIC ACID
    2. Synonyms: (4-ETHOXY-3-NITROPHENYL)ACETIC ACID;4-ETHOXY-3-NITRO-BENZENEACETIC ACID;BENZENEACETIC ACID, 4-ETHOXY-3-NITRO-;VAJLZGXUIFUUHK-UHFFFAOYSA-N
    3. CAS NO:373361-54-7
    4. Molecular Formula: C10H11NO5
    5. Molecular Weight: 225.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 373361-54-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4-ETHOXY-3-NITROPHENYL)ACETIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-ETHOXY-3-NITROPHENYL)ACETIC ACID(373361-54-7)
    11. EPA Substance Registry System: (4-ETHOXY-3-NITROPHENYL)ACETIC ACID(373361-54-7)
  • 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: 373361-54-7(Hazardous Substances Data)

373361-54-7 Usage

Uses

Used in Pharmaceutical Synthesis:
(4-ETHOXY-3-NITROPHENYL)ACETIC ACID is used as an intermediate in the synthesis of pharmaceuticals for its potential role in the development of new drugs. Its unique structure allows for the creation of a wide range of medicinal compounds.
Used in Agrochemical Production:
In the agrochemical industry, (4-ETHOXY-3-NITROPHENYL)ACETIC ACID is used as an intermediate in the production of various agrochemicals, contributing to the development of innovative products for agricultural applications.
Used in Organic Compound Production:
(4-ETHOXY-3-NITROPHENYL)ACETIC ACID serves as an intermediate in the production of a variety of organic compounds, showcasing its utility in the field of organic chemistry.
Used in Industrial Applications:
While further research is necessary to fully understand its potential, (4-ETHOXY-3-NITROPHENYL)ACETIC ACID may also have applications in various industrial processes, adding to its value as a versatile chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 373361-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,3,3,6 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 373361-54:
(8*3)+(7*7)+(6*3)+(5*3)+(4*6)+(3*1)+(2*5)+(1*4)=147
147 % 10 = 7
So 373361-54-7 is a valid CAS Registry Number.

373361-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-ETHOXY-3-NITROPHENYL)ACETIC ACID

1.2 Other means of identification

Product number -
Other names 4-ethoxy-3-nitrophenylacetic 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:373361-54-7 SDS

373361-54-7Upstream product

373361-54-7Relevant articles and documents

INDAZOLES SUBSTITUTED WITH1,1-DIOXOISOTHIAZOLIDINE USEFUL AS INHIBITORS OF CELL PROLIFERATION

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, (2008/06/13)

The present invention relates to an indazole derivative, pharmaceutically acceptable salt, solvated product and isomer thereof substituted with 1,1-dioxoisothiazolidine which are useful as inhibitors for Cyclin Dependent Kinase (CDK). The present inventio

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