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1-(5-chloropyridin-2-yl)propan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1536438-57-9 Structure
  • Basic information

    1. Product Name: 1-(5-chloropyridin-2-yl)propan-1-one
    2. Synonyms:
    3. CAS NO:1536438-57-9
    4. Molecular Formula:
    5. Molecular Weight: 169.611
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1536438-57-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(5-chloropyridin-2-yl)propan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(5-chloropyridin-2-yl)propan-1-one(1536438-57-9)
    11. EPA Substance Registry System: 1-(5-chloropyridin-2-yl)propan-1-one(1536438-57-9)
  • 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: 1536438-57-9(Hazardous Substances Data)

1536438-57-9 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

It is derived from the parent compound pyridine, which is a heterocyclic aromatic organic compound.

Explanation

The compound has a carbonyl group attached to two alkyl groups, and a pyridine ring with a chlorine atom substitution.

Explanation

It is classified as a ketone due to the presence of a carbonyl group attached to two alkyl groups.

Explanation

The pyridine ring in the compound has a chlorine atom attached, which influences its reactivity and properties.

Explanation

The compound is used in the synthesis of various organic compounds and is also studied for its potential applications in the development of new drugs and materials.

Explanation

The reactivity of 1-(5-chloropyridin-2-yl)propan-1-one is crucial for determining its suitability in various chemical reactions and its potential use in drug development and material science.

Explanation

The synthesis process of the compound is essential for understanding its properties, reactivity, and potential applications in various fields.

Derivative of pyridine

Yes

Chemical structure

Contains a carbonyl group (C=O) and a pyridine ring

Type of compound

Ketone

Substitution

Chlorine atom on the pyridine ring

Applications

Organic synthesis and pharmaceutical research

Reactivity

Important for understanding potential applications

Synthesis

Key for studying the compound's properties and applications

Check Digit Verification of cas no

The CAS Registry Mumber 1536438-57-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,6,4,3 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1536438-57:
(9*1)+(8*5)+(7*3)+(6*6)+(5*4)+(4*3)+(3*8)+(2*5)+(1*7)=179
179 % 10 = 9
So 1536438-57-9 is a valid CAS Registry Number.

1536438-57-9Downstream Products

1536438-57-9Relevant articles and documents

3-(6-CHLORO-3-OXO-3,4-DIHYDRO-(2H)-1,4-BENZOXAZIN-4-YL) PROPANOIC ACID DERIVATIVES AND THEIR USE AS KMO INHIBITORS

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Page/Page column 24; 25, (2016/12/22)

Compounds of formula (I) wherein: R1 is heteroaryl optionally substituted by methyl, ethyl, halo or =O; and R2 is H, methyl or ethyl. and salts thereof are KMO inhibitors and may be useful in the treatment of various disorders, for example acute pancreatitis, chronic kidney disease, other conditions associated with systemic inflammatory response syndrome (SIRS), Huntington's disease, Alzheimer's disease, spinocerebellar ataxias, Parkinson's disease, AIDS-dementia complex, HIV infection, amylotrophic lateral sclerosis (ALS), depression, schizophrenia, sepsis, cardiovascular shock, severe trauma, acute lung injury, acute respiratory distress syndrome, acute cholecystitis, severe burns, pneumonia, extensive surgical procedures, ischemic bowel disease, severe acute hepatic disease, severe acute hepatic encephalopathy or acute renal failure.

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