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1-(7-Hydroxy[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 932736-65-7 Structure
  • Basic information

    1. Product Name: 1-(7-Hydroxy[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-ethanone
    2. Synonyms: 1-(7-Hydroxy[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-ethanone
    3. CAS NO:932736-65-7
    4. Molecular Formula: C7H6N4O2
    5. Molecular Weight: 178.14814
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 932736-65-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(7-Hydroxy[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(7-Hydroxy[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-ethanone(932736-65-7)
    11. EPA Substance Registry System: 1-(7-Hydroxy[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-ethanone(932736-65-7)
  • 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: 932736-65-7(Hazardous Substances Data)

932736-65-7 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 6 carbon (C), 6 hydrogen (H), 4 nitrogen (N), and 2 oxygen (O) atoms.

Explanation

This describes the arrangement of atoms and the functional groups present in the molecule. The compound is a derivative of the triazolopyrimidine group, which is fused with a pyrimidine ring, and contains a hydroxyl group and an ethanone moiety.

Explanation

The systematic name follows the IUPAC nomenclature rules, providing a standardized way to name chemical compounds. It describes the specific arrangement of atoms and functional groups in the molecule.

Explanation

The hydroxyl group (-OH) is a polar functional group that can form hydrogen bonds, while the ethanone moiety (-CO-CH3) is a carbonyl group attached to an ethyl group, which can participate in various chemical reactions.

Explanation

The compound is derived from the triazolopyrimidine group, which is a fused ring system consisting of a triazole and a pyrimidine. This group is known for its diverse biological activities and potential applications in drug development.
6. Potential Pharmacological Activities

Explanation

The compound may exhibit pharmacological activities due to its unique structure and functional groups. These activities could be relevant for the development of new drugs or therapeutic agents.

Explanation

The compound can be used in various research applications, including the study of its chemical properties, reactivity, and potential interactions with biological targets.
8. Context-Dependent Properties, Uses, and Risks

Explanation

The specific properties, uses, and potential risks of the compound will depend on the context in which it is being considered, such as the intended application, concentration, and environmental conditions.

Structure

1-(7-Hydroxy[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-ethanone

Functional Groups

Hydroxyl group, Ethanone moiety

Derivative

Triazolopyrimidine group

Research Applications

Chemical and biological research

Check Digit Verification of cas no

The CAS Registry Mumber 932736-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,2,7,3 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 932736-65:
(8*9)+(7*3)+(6*2)+(5*7)+(4*3)+(3*6)+(2*6)+(1*5)=187
187 % 10 = 7
So 932736-65-7 is a valid CAS Registry Number.

932736-65-7Downstream Products

932736-65-7Relevant articles and documents

Recyclization of condensed carbethoxypyrimidines accompanied by substitution of a carbon atom into the heterocycle

Danagulyan,Mkrtchyan,Panosyan

, p. 485 - 491 (2007/10/03)

Condensation in ethanol of ethyl ethoxymethyleneacetoacetate with systems containing an amidine fragment (substituted 3-aminopyrazoles and 3-amino-1,2,4-triazole) gave 6-carbethoxy-7-methylpyrazolo[1,5-a]pyrimidines. Addition of base to solutions of the o

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