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3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol is a pyrazole derivative chemical compound characterized by the molecular formula C6H6F3NO. It features a trifluoromethyl group and a hydroxyl group attached to the pyrazole ring, endowing it with unique chemical properties and reactivity.

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  • 1001020-13-8 Structure
  • Basic information

    1. Product Name: 3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol
    2. Synonyms: 3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol;(3-TrifluoroMethyl-1H-pyrazol-4-yl)Methanol;4-(HydroxyMethyl)-3-(TrifluoroMethyl)pyrazole;[5-(trifluoromethyl)-1H-pyrazol-4-yl]methanol;(3-Trifluoromethyl-1H-pyrazol-4-yl)
    3. CAS NO:1001020-13-8
    4. Molecular Formula: C5H5F3N2O
    5. Molecular Weight: 166.1012096
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1001020-13-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 273.4±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.533±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 10.34±0.50(Predicted)
    10. CAS DataBase Reference: 3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol(1001020-13-8)
    12. EPA Substance Registry System: 3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol(1001020-13-8)
  • 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: 1001020-13-8(Hazardous Substances Data)

1001020-13-8 Usage

Uses

Used in Organic Synthesis:
3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol is used as a reagent in organic synthesis for its distinctive chemical structure and reactivity, facilitating the creation of various complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol is utilized as a reagent in the development of new drugs and pharmaceutical products, leveraging its unique properties to enhance drug discovery and design processes.
Used as an Intermediate in Chemical Production:
3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol may also serve as an intermediate in the production of other chemicals and materials, contributing to the synthesis of a wide range of compounds across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1001020-13-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,0,2 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1001020-13:
(9*1)+(8*0)+(7*0)+(6*1)+(5*0)+(4*2)+(3*0)+(2*1)+(1*3)=28
28 % 10 = 8
So 1001020-13-8 is a valid CAS Registry Number.

1001020-13-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-(trifluoromethyl)-1H-pyrazol-4-yl]methanol

1.2 Other means of identification

Product number -
Other names (3-(Trifluoromethyl)-1H-pyrazol-4-yl)methanol

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:1001020-13-8 SDS

1001020-13-8Relevant articles and documents

SUBSTITUTED BICYCLE HETEROCYCLIC DERIVATIVES USEFUL AS ROMK CHANNEL INHIBITORS

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Page/Page column 173; 174, (2018/06/06)

Disclosed are compounds of Formula (I) or a salt thereof, wherein R1 is (II) or (III); each W is independently NR1b or O; Z is a bond or CHR1d; and R1, R2, Rd, R3, L1, L2, R1a, R1b, R1c, and n are define herein. Also disclosed are methods of using such compounds as inhibitors of ROMK, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating cardiovascular diseases.

HETEROCYCLIC DERIVATIVES

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Page/Page column 7-8, (2009/05/28)

The present invention relates to a heterocyclic derivative according to formula I wherein the variables are defined as in the specification, or to a pharmaceutically acceptable salt or solvate thereof. The present invention also relates to a pharmaceutica

PYRAZOLEALKANAMIDE SUBSTITUTED THIOPHENES AS AMPA POTENTIATORS

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Page/Page column 52-53, (2008/06/13)

The present invention relates to a heterocyclic derivative according to Formula (I) wherein the variables are defined as in the specification, or to a pharmaceutically acceptable salt or solvate thereof. The present invention also relates to a pharmaceuti

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