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110356-26-8

1H-Pyrazole-3-carboxylicacid, 4-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 110356-26-8 Structure

  • Basic information

    1. Product Name: 1H-Pyrazole-3-carboxylicacid, 4-(4-methoxyphenyl)-
    2. Synonyms: Pyrazole-3(or5)-carboxylic acid, 4-(p-methoxyphenyl)- (6CI)
    3. CAS NO:110356-26-8
    4. Molecular Formula: C11H10 N2 O3
    5. Molecular Weight: 218.212
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 110356-26-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1H-Pyrazole-3-carboxylicacid, 4-(4-methoxyphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Pyrazole-3-carboxylicacid, 4-(4-methoxyphenyl)-(110356-26-8)
    11. EPA Substance Registry System: 1H-Pyrazole-3-carboxylicacid, 4-(4-methoxyphenyl)-(110356-26-8)

  • 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: 110356-26-8(Hazardous Substances Data)

110356-26-8 Usage

Substituent of 4-(4-methoxyphenyl)

The presence of this substituent group on the pyrazole and carboxylic acid derivative influences the compound's chemical properties and potential therapeutic applications.

Pharmaceutical research

1H-Pyrazole-3-carboxylic acid, 4-(4-methoxyphenyl)is commonly used in pharmaceutical research, indicating its potential for development in the field of medicine.

Potential therapeutic applications

The compound has been studied for its potential use in the development of new drugs, particularly those with anti-inflammatory and analgesic properties.

Anti-inflammatory properties

The compound may have the ability to reduce inflammation, which is a key factor in many diseases and conditions.

Analgesic properties

The compound may also have the ability to relieve pain, making it a potential candidate for pain management applications.

Promising candidate for further research

Due to its structure and properties, 1H-Pyrazole-3-carboxylic acid, 4-(4-methoxyphenyl)is considered a promising candidate for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 110356-26-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,3,5 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110356-26:
(8*1)+(7*1)+(6*0)+(5*3)+(4*5)+(3*6)+(2*2)+(1*6)=78
78 % 10 = 8
So 110356-26-8 is a valid CAS Registry Number.

110356-26-8SDS

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-(4-methoxyphenyl)-1H-pyrazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-(4-Methoxyphenyl)-pyrazol-3-carbonsaeure

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:110356-26-8 SDS

110356-26-8Relevant articles and documents

Pyrazole-3/5-carboxylic acids from 3/5-trifluoromethyl NH-pyrazoles

Ermolenko, Mikhail S.,Guillou, Sandrine,Janin, Yves L.

, p. 257 - 263 (2013/01/15)

We report here the transformation of 3/5-trifluoromethylpyrazoles derivative into the corresponding NH-pyrazole-3/5-carboxylic acids. Moreover, from 4- or 5-iodinated-3/5-trifluoromethylpyrazoles building blocks and the use of Suzuki-Miyaura or Negishi reactions followed by the trifluoromethyl hydrolysis, we illustrate short and original accesses to many series of NH-pyrazole-3/5-carboxylic acids otherwise difficult to prepare.

NEW EFFICIENT SYNTHESIS OF 3(5)-CARBOMETHOXY-4-ARYLPYRAZOLES FROM 3-ARYL-2,3-DEHYDROAMINO ACID DERIVATIVES

Catiela, Carlos,Villegas, M. Dolores Diaz de,Gainza, M. Pilar

, p. 165 - 172 (2007/10/02)

3(5)-Carbomethoxy-4-arylpyrazoles can be easily obtained by aromatization with boron trifluoride etherate of 4-aryl-3-acetamido(or benzamido)-3-carbomethoxy-Δ1-pyrazolines synthesized by 1,3-dipolar cycloaddition of diazomethane with 3-aryl-2,3

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