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(5-Amino-1H-pyrazol-3-yl)Methanol is a chemical compound that belongs to the class of aminopyrazoles. It is a derivative of the parent compound pyrazole, characterized by the presence of a hydroxyl group (-OH) attached to the 3rd carbon atom and an amino group (-NH2) at the 5th carbon atom. This unique structure and the functional groups it possesses make it a valuable intermediate in the synthesis of various pharmaceutical compounds and a promising candidate for use in medicinal chemistry.

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  • 1000895-26-0 Structure
  • Basic information

    1. Product Name: (5-AMino-1H-pyrazol-3-yl)Methanol
    2. Synonyms: (5-AMino-1H-pyrazol-3-yl)Methanol;5-amino-1H-Pyrazole-3-methanol;(5-amino-1H-pyrazol-3-yl)methanol/(3-amino-1H-pyrazol-5-yl)methanol
    3. CAS NO:1000895-26-0
    4. Molecular Formula: C4H7N3O
    5. Molecular Weight: 113.11788
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1000895-26-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 456.1±30.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.467±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. PKA: 13.52±0.10(Predicted)
    10. CAS DataBase Reference: (5-AMino-1H-pyrazol-3-yl)Methanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: (5-AMino-1H-pyrazol-3-yl)Methanol(1000895-26-0)
    12. EPA Substance Registry System: (5-AMino-1H-pyrazol-3-yl)Methanol(1000895-26-0)
  • 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: 1000895-26-0(Hazardous Substances Data)

1000895-26-0 Usage

Uses

Used in Medicinal Chemistry:
(5-Amino-1H-pyrazol-3-yl)Methanol is used as a building block for the synthesis of pharmaceutical compounds due to its unique structure and functional groups. It contributes to the development of biologically active molecules, which can be utilized in the creation of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, (5-Amino-1H-pyrazol-3-yl)Methanol serves as a versatile intermediate. Its presence allows for the formation of a wide range of chemical products, expanding the scope of chemical reactions and the types of compounds that can be synthesized.
Used as a Research Reagent:
(5-Amino-1H-pyrazol-3-yl)Methanol is also used as a research reagent in chemical and biochemical studies. Its unique properties make it suitable for investigating various chemical reactions and mechanisms, contributing to a deeper understanding of chemical processes and the development of new methodologies in the field.

Check Digit Verification of cas no

The CAS Registry Mumber 1000895-26-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,8,9 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1000895-26:
(9*1)+(8*0)+(7*0)+(6*0)+(5*8)+(4*9)+(3*5)+(2*2)+(1*6)=110
110 % 10 = 0
So 1000895-26-0 is a valid CAS Registry Number.

1000895-26-0SDS

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 3-amino-5-hydroxymethyl-1H-pyrazole

1.2 Other means of identification

Product number -
Other names (5-Amino-1H-pyrazol-3-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:1000895-26-0 SDS

1000895-26-0Downstream Products

1000895-26-0Relevant articles and documents

Novel Compounds

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Page/Page column 50, (2008/06/13)

There is provided a compound of formula (I): processes for the manufacture thereof, pharmaceutical compositions thereof and uses in therapy.

QUINOLINE DERIVATIVES

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Page/Page column 116, (2008/06/13)

The invention concerns quinoline derivatives of Formula (I): or a pharmaceutically-acceptable salt thereof, wherein each of X1, p, R1, q, R2, R3, R4, R5, Ring A, r and R6 has any of the meanings defined hereinbefore in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use in the treatment of cell proliferative disorders.

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