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2-(1H-pyrazol-1-yl)propan-1-ol, commonly referred to as pyrazolol, is a synthetic organic compound with the molecular formula C6H9N3O. It is a member of the pyrazole derivatives class, known for its pyrazole ring structure and a propanol side chain. Pyrazolol is utilized in the pharmaceutical industry as a building block for the synthesis of various drugs and bioactive molecules due to its unique pharmacological properties. Its versatility extends to its use as a reagent in organic synthesis and as a ligand in coordination chemistry, making it a valuable asset for researchers in organic and pharmaceutical chemistry.

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  • 191725-73-2 Structure
  • Basic information

    1. Product Name: 2-(1H-pyrazol-1-yl)propan-1-ol
    2. Synonyms: 2-(1H-pyrazol-1-yl)propan-1-ol;02(3-Pyrazol-1-yl-phenyl)-methanol;Albb-004087;2-(1H-pyrazol-1-yl)-1-propanol(SALTDATA: FREE);2-(1H-Pyrazol-1-yl)-1-propanol
    3. CAS NO:191725-73-2
    4. Molecular Formula: C6H10N2O
    5. Molecular Weight: 126.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 191725-73-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 225.2°C at 760 mmHg
    3. Flash Point: 90°C
    4. Appearance: /
    5. Density: 1.12g/cm3
    6. Vapor Pressure: 0.0499mmHg at 25°C
    7. Refractive Index: 1.541
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(1H-pyrazol-1-yl)propan-1-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(1H-pyrazol-1-yl)propan-1-ol(191725-73-2)
    12. EPA Substance Registry System: 2-(1H-pyrazol-1-yl)propan-1-ol(191725-73-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 191725-73-2(Hazardous Substances Data)

191725-73-2 Usage

Uses

Used in Pharmaceutical Industry:
2-(1H-pyrazol-1-ol)propan-1-ol is used as a building block for the synthesis of various drugs and bioactive molecules, leveraging its pyrazole ring structure and propanol side chain to contribute to the development of new pharmaceutical agents.
Used in Organic Synthesis:
Pyrazolol is employed as a reagent in organic synthesis, where its unique chemical properties facilitate the creation of a range of organic compounds for various applications.
Used in Coordination Chemistry:
In coordination chemistry, 2-(1H-pyrazol-1-yl)propan-1-ol is used as a ligand, participating in the formation of coordination compounds that have potential applications in various fields, including catalysis and materials science.
Used in Drug Development:
Pyrazolol has potential applications in drug development, where its properties can be harnessed to design and synthesize new therapeutic agents with improved pharmacological profiles.
Used in Medicinal Chemistry:
As a valuable tool for researchers, pyrazolol is utilized in medicinal chemistry to explore its potential in the discovery and optimization of bioactive molecules for therapeutic use.

Check Digit Verification of cas no

The CAS Registry Mumber 191725-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,7,2 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 191725-73:
(8*1)+(7*9)+(6*1)+(5*7)+(4*2)+(3*5)+(2*7)+(1*3)=152
152 % 10 = 2
So 191725-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2O/c1-6(5-9)8-4-2-3-7-8/h2-4,6,9H,5H2,1H3

191725-73-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyrazol-1-ylpropan-1-ol

1.2 Other means of identification

Product number -
Other names 2-Pyrazol-1-yl-propan-1-ol

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:191725-73-2 SDS

191725-73-2Downstream Products

191725-73-2Relevant articles and documents

SMALL MOLECULE MODULATORS OF IL-17

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Page/Page column 30-31, (2022/01/05)

The present invention relates to a compound according to formula (I) and pharmaceutically acceptable salts, hydrates, or solvates thereof. The invention further relates to said compounds for use in therapy, to pharmaceutical compositions comprising said compounds, to methods of treating diseases, e.g. dermal diseases, with said compounds, and to the use of said compounds in the manufacture of medicaments.

Y(NO3)3·6H2O catalyzed regioselective ring opening of epoxides with aliphatic, aromatic, and heteroaromatic amines

Bhanushali, Mayur J.,Nandurkar, Nitin S.,Bhor, Malhari D.,Bhanage, Bhalchandra M.

, p. 3672 - 3676 (2008/09/19)

Yttrium nitrate hexahydrate [Y(NO3)3·6H2O] was found to be an efficient catalyst for selective ring opening of epoxides with aliphatic, aromatic, and heteroaromatic amines at room temperature under solvent-free conditions. The system tolerated a variety of hindered and functionalized epoxides/amines and afforded the desired β-amino alcohols at low catalyst concentration.

Piperidine and tetrahydropyridine derivatives

-

, (2008/06/13)

A class of substituted piperidine and tetrahydropyridine derivatives, linked through the 4-position thereof via an alkylene chain to a fused bicyclic heteroaromatic moiety such as indolyl, and further substituted at the 1-position by an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl-alkyl, aryl-alkyl or heteroaryl-alkyl moiety, are selective agonists of 5-HT1 -like receptors, being potent agonists of the human 5-HT1Dα; receptor subtype whilst processing at least a 10-fold selective affinity for the 5-HT1Dα; receptor subtype relative to the 5-HT1Dβ; subtype; they are therefore useful in the treatment and/or prevention of clinical conditions, in particular migraine and associated disorders, for which a subtype-selective agonist of 5-HT1D receptors is indicated, whilst eliciting fewer side-effects, notably adverse cardiovascular events, than those associated with non-subtype-selective 5-HT1D receptor agonists.

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