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139329-90-1

Ethyl 3-acetamido-5-chloro-2-hydroxybenzoate is a chemical compound with the molecular formula C12H12ClNO4. It is a derivative of salicylic acid, featuring an acetamido group and a 5-chloro-2-hydroxybenzoate moiety. Ethyl 3-acetamido-5-chloro-2-hydroxybenzoate holds potential pharmaceutical applications due to its capacity to inhibit prostaglandin synthesis, which plays a role in inflammation and pain signaling.

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  • 139329-90-1 Structure

  • Basic information

    1. Product Name: Ethyl 3-acetamido-5-chloro-2-hydroxybenzoate
    2. Synonyms: Ethyl 3-acetamido-5-chloro-2-hydroxybenzoate
    3. CAS NO:139329-90-1
    4. Molecular Formula: C11H12ClNO4
    5. Molecular Weight: 257.67028
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 139329-90-1.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.: Inert atmosphere,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethyl 3-acetamido-5-chloro-2-hydroxybenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethyl 3-acetamido-5-chloro-2-hydroxybenzoate(139329-90-1)
    11. EPA Substance Registry System: Ethyl 3-acetamido-5-chloro-2-hydroxybenzoate(139329-90-1)

  • 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: 139329-90-1(Hazardous Substances Data)

139329-90-1 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 3-acetamido-5-chloro-2-hydroxybenzoate is used as an analgesic and anti-inflammatory agent for the treatment of various conditions such as arthritis, muscle pain, and headaches. Its ability to inhibit prostaglandin synthesis contributes to its effectiveness in managing pain and reducing inflammation.
The ethyl ester form of this compound enhances its solubility and bioavailability, which is advantageous for drug development and delivery. This characteristic makes Ethyl 3-acetamido-5-chloro-2-hydroxybenzoate a promising candidate for the creation of new pharmaceuticals aimed at treating inflammatory and painful conditions more effectively.
However, further research is necessary to fully understand its pharmacological properties and to assess any potential side effects that may accompany its use. This research will be critical in advancing the compound's application in medicinal chemistry and ensuring its safety and efficacy for patients.

Check Digit Verification of cas no

The CAS Registry Mumber 139329-90-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,3,2 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 139329-90:
(8*1)+(7*3)+(6*9)+(5*3)+(4*2)+(3*9)+(2*9)+(1*0)=151
151 % 10 = 1
So 139329-90-1 is a valid CAS Registry Number.

139329-90-1SDS

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 N-(3-ethoxycarbonyl-5-chloro-2-hydroxyphenyl)acetamide

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 -
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More Details:139329-90-1 SDS

139329-90-1Relevant articles and documents

Design and synthesis of 6-chloro-3,4-dihydro-4-methyl-2H-1,4-benzoxazine-8-carboxamide derivatives as potent serotonin-3 (5-HT3) receptor antagonists

Kuroita, Takanobu,Sakamori, Masamitsu,Kawakita, Takeshi

, p. 756 - 764 (2007/10/03)

Several 3-substituted 5-chloro-2-methoxybenzamides were synthesized and evaluated for serotonin-3 (5-HT3) receptor binding affinity. The 5-HT3 receptor antagonistic activity of zacopride, a representative 5-HT3 receptor an

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