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1-(4-methoxyphenyl)-5-(1H-pyrrol-1-yl)-1H-pyrazole-4-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1-(4-Methoxyphenyl)-5-(1H-pyrrol-1-yl)-1H-pyrazole-4-carboxylic acid

    Cas No: 116834-10-7

  • USD $ 1.9-2.9 / Gram

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  • 116834-10-7 Structure
  • Basic information

    1. Product Name: 1-(4-methoxyphenyl)-5-(1H-pyrrol-1-yl)-1H-pyrazole-4-carboxylic acid
    2. Synonyms:
    3. CAS NO:116834-10-7
    4. Molecular Formula: C15H13N3O3
    5. Molecular Weight: 283.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116834-10-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 497.3°C at 760 mmHg
    3. Flash Point: 254.6°C
    4. Appearance: N/A
    5. Density: 1.31g/cm3
    6. Vapor Pressure: 1.04E-10mmHg at 25°C
    7. Refractive Index: 1.644
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(4-methoxyphenyl)-5-(1H-pyrrol-1-yl)-1H-pyrazole-4-carboxylic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(4-methoxyphenyl)-5-(1H-pyrrol-1-yl)-1H-pyrazole-4-carboxylic acid(116834-10-7)
    12. EPA Substance Registry System: 1-(4-methoxyphenyl)-5-(1H-pyrrol-1-yl)-1H-pyrazole-4-carboxylic acid(116834-10-7)
  • 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: 116834-10-7(Hazardous Substances Data)

116834-10-7 Usage

Chemical structure

The compound consists of a pyrazole ring fused to a pyrrole ring, with a carboxylic acid group attached at the 4-position of the pyrazole ring and a methoxyphenyl group at the 1-position.

Molecular weight

Approximately 267.28 g/mol

Functional groups

Carboxylic acid, pyrazole, pyrrole, and methoxyphenyl

Potential pharmaceutical applications

Due to its unique structure and properties, the compound may have biological activities such as anti-inflammatory, antitumor, or antimicrobial effects.

Research and development

Further research and development of this compound could lead to the discovery of new drugs for various medical conditions.

Solubility

The compound's solubility properties are not explicitly mentioned in the provided material, but it is likely to be soluble in polar solvents such as water, methanol, or ethanol due to the presence of the carboxylic acid group.

Stability

The stability of the compound is not explicitly mentioned in the provided material, but it may be sensitive to heat, light, or moisture due to the presence of the carboxylic acid and methoxyphenyl groups.

Check Digit Verification of cas no

The CAS Registry Mumber 116834-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,8,3 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116834-10:
(8*1)+(7*1)+(6*6)+(5*8)+(4*3)+(3*4)+(2*1)+(1*0)=117
117 % 10 = 7
So 116834-10-7 is a valid CAS Registry Number.

116834-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methoxyphenyl)-5-pyrrol-1-ylpyrazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names BB_SC-9113

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:116834-10-7 SDS

116834-10-7Relevant articles and documents

Synthesis of novel pyrazolopyrrolopyrazines, potential analogs of sildenafil

Kopp,Lancelot,Dallemagne,Rault

, p. 1045 - 1050 (2007/10/03)

Synthesis of novel pyrazolopyrrolopyrazines is herein described with the aim to reach new specific PDE-5 inhibitors of potential clinical interest in male erectile dysfunction.

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