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Pyridine, 3-chloro-5-(phenylmethoxy)is a chemical compound with the molecular formula C12H9ClNO. It is a derivative of pyridine and contains a chlorine atom at the 3rd position and a phenylmethoxy group at the 5th position of the pyridine ring.

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  • 251996-81-3 Structure
  • Basic information

    1. Product Name: PYRIDINE, 3-CHLORO-5-(PHENYLMETHOXY)-
    2. Synonyms: 3-CHLORO-5-(PHENYLMETHOXY)-PYRIDINE;PYRIDINE, 3-CHLORO-5-(PHENYLMETHOXY)-;3-(benzyloxy)-5-chloropyridine
    3. CAS NO:251996-81-3
    4. Molecular Formula: C12H10ClNO
    5. Molecular Weight: 219.67
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 251996-81-3.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: PYRIDINE, 3-CHLORO-5-(PHENYLMETHOXY)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: PYRIDINE, 3-CHLORO-5-(PHENYLMETHOXY)-(251996-81-3)
    11. EPA Substance Registry System: PYRIDINE, 3-CHLORO-5-(PHENYLMETHOXY)-(251996-81-3)
  • 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: 251996-81-3(Hazardous Substances Data)

251996-81-3 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
Pyridine, 3-chloro-5-(phenylmethoxy)is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a wide range of compounds with potential therapeutic and pesticidal properties.
Used in Organic Chemistry:
Pyridine, 3-chloro-5-(phenylmethoxy)is used as a building block in organic chemistry reactions to introduce the pyridine ring and the phenylmethoxy group into more complex molecules. This enables the development of new compounds with specific functions and applications.
Used in Organic Synthesis and Medicinal Chemistry Research:
Pyridine, 3-chloro-5-(phenylmethoxy)is used as a reagent in organic synthesis and medicinal chemistry research. Its presence in reactions can lead to the formation of novel compounds with potential applications in various fields, including drug discovery and development.
It is important to follow proper handling and storage procedures to ensure the safe use of Pyridine, 3-chloro-5-(phenylmethoxy)-.

Check Digit Verification of cas no

The CAS Registry Mumber 251996-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,9,9 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 251996-81:
(8*2)+(7*5)+(6*1)+(5*9)+(4*9)+(3*6)+(2*8)+(1*1)=173
173 % 10 = 3
So 251996-81-3 is a valid CAS Registry Number.
InChI:InChI=1S/C12H10ClNO/c13-11-6-12(8-14-7-11)15-9-10-4-2-1-3-5-10/h1-8H,9H2

251996-81-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Benzyloxy)-5-chloropyridine

1.2 Other means of identification

Product number -
Other names 5-Chloro-3-benzyloxypyridine

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:251996-81-3 SDS

251996-81-3Relevant articles and documents

A versatile method for suzuki cross-coupling reactions of nitrogen heterocycles

Kudo, Noriaki,Perseghini, Mauro,Fu, Gregory C.

, p. 1282 - 1284 (2007/10/03)

(Chemical Equation Presented) A wide-ranging study of Suzuki reactions which use nitrogen-containing heterocycles is described (see scheme; dba = dibenzylideneacetone, Cy = cyclohexyl). This method is highly versatile (a single procedure was used for all substrates, including boronate esters and trifluoroborates), compatible with a variety of unprotected functionalities (e.g., NH2-and OH-substituted substrates), and efficient even with unactivated aryl chlorides.

Cell adhesion-inhibiting antiinflammatory compounds

-

, (2008/06/13)

Compounds having Formula I are useful for treating inflammation. Also disclosed are pharmaceutical compositions comprising compounds of Formula I, and methods of inhibiting/treating inflammatory diseases in a mammal.

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