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5-THIEN-2-YL-4H-PYRAZOLE-3-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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  • 182415-24-3 Structure
  • Basic information

    1. Product Name: 5-THIEN-2-YL-4H-PYRAZOLE-3-CARBOXYLIC ACID
    2. Synonyms: 5-(2-THIENYL)-3-PYRAZOLECARBOXYLIC ACID;5-(2-THIENYL)PYRAZOLE-3-CARBOXYLIC ACID;5-THIEN-2-YL-1H-PYRAZOLE-3-CARBOXYLIC ACID;5-THIEN-2-YL-4H-PYRAZOLE-3-CARBOXYLIC ACID;5-THIOPHEN-2-YL-1H-PYRAZOLE-3-CARBOXYLIC ACID;AKOS PAO-0367;5-THIOPHEN-2-YL-1H-PYRAZOLE-3-CARBOXYLIC ACID, 95+%;5-(Thiophen-2-yl)-1H-pyrazole-3-carboxylic acid ,97%
    3. CAS NO:182415-24-3
    4. Molecular Formula: C8H6N2O2S
    5. Molecular Weight: 194.21
    6. EINECS: N/A
    7. Product Categories: Carboxylic Acids;Pyrazoles & Triazoles
    8. Mol File: 182415-24-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 509.4 °C at 760 mmHg
    3. Flash Point: 261.8 °C
    4. Appearance: /
    5. Density: 1.514 g/cm3
    6. Vapor Pressure: 3.38E-11mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-THIEN-2-YL-4H-PYRAZOLE-3-CARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-THIEN-2-YL-4H-PYRAZOLE-3-CARBOXYLIC ACID(182415-24-3)
    12. EPA Substance Registry System: 5-THIEN-2-YL-4H-PYRAZOLE-3-CARBOXYLIC ACID(182415-24-3)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 22-36/37/38
    3. Safety Statements: 22-26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 182415-24-3(Hazardous Substances Data)

182415-24-3 Usage

Chemical Properties

Off-white to light yellow solid

Check Digit Verification of cas no

The CAS Registry Mumber 182415-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,4,1 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 182415-24:
(8*1)+(7*8)+(6*2)+(5*4)+(4*1)+(3*5)+(2*2)+(1*4)=123
123 % 10 = 3
So 182415-24-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O2S/c11-8(12)6-4-5(9-10-6)7-2-1-3-13-7/h1-4H,(H,9,10)(H,11,12)/p-1

182415-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-thiophen-2-yl-1H-pyrazole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-Thien-2-yl-1H-pyrazole-3-carboxylic 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:182415-24-3 SDS

182415-24-3Downstream Products

182415-24-3Relevant articles and documents

Design, synthesis, biological evaluation and in silico studies of pyrazole‐based nh2‐acyl oseltamivir analogues as potent neuraminidase inhibitors

Ye, Jiqing,Lin, Lin,Xu, Jinyi,Chan, Paul Kay-Sheung,Yang, Xiao,Ma, Cong

, (2021/05/05)

Oseltamivir represents one of the most successful neuraminidase (NA) inhibitors in the current anti‐influenza therapy. The 150‐cavity of NA was identified as an additional binding pocket, and novel NA inhibitors have been designed to occupy the 150‐cavity

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.

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