Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Pyridinium, chlorophenylmethylide, with the molecular formula C11H11N, is a pyridinium salt featuring a chlorophenylmethyl group. It is recognized for its strong electrophilic properties, making it a valuable reactant in organic synthesis. This versatile compound is instrumental in the creation of heterocyclic compounds and the formation of new carbon-carbon and carbon-nitrogen bonds, significantly contributing to the advancement of pharmaceuticals, agrochemicals, and materials.

115732-59-7 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 115732-59-7 Structure
  • Basic information

    1. Product Name: Pyridinium, chlorophenylmethylide
    2. Synonyms:
    3. CAS NO:115732-59-7
    4. Molecular Formula: C12H10ClN
    5. Molecular Weight: 203.671
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115732-59-7.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: Pyridinium, chlorophenylmethylide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyridinium, chlorophenylmethylide(115732-59-7)
    11. EPA Substance Registry System: Pyridinium, chlorophenylmethylide(115732-59-7)
  • 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: 115732-59-7(Hazardous Substances Data)

115732-59-7 Usage

Uses

Used in Organic Synthesis:
Pyridinium, chlorophenylmethylide is used as a reactant for its strong electrophilic nature, facilitating various chemical reactions and contributing to the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, Pyridinium, chlorophenylmethylide is utilized as a building block for the development of new drugs, owing to its ability to form heterocyclic compounds and new carbon-carbon and carbon-nitrogen bonds, which are essential for creating novel medicinal agents.
Used in Agrochemical Production:
Pyridinium, chlorophenylmethylide also serves as a key component in the synthesis of agrochemicals, where its reactivity and capacity to form new bonds are harnessed to produce effective compounds for agricultural applications.
Used in Material Science:
In the field of material science, Pyridinium, chlorophenylmethylide is employed in the development of new materials, capitalizing on its versatility to create innovative substances with unique properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 115732-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,3 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115732-59:
(8*1)+(7*1)+(6*5)+(5*7)+(4*3)+(3*2)+(2*5)+(1*9)=117
117 % 10 = 7
So 115732-59-7 is a valid CAS Registry Number.

115732-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name phenylchloropyridinium ylide

1.2 Other means of identification

Product number -
Other names -

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:115732-59-7 SDS

115732-59-7Relevant articles and documents

Formation of Indolizines by the Addition of α-Chloroacrylonitrile to Pyridinium Ylides: Regioselectivity and Hammett Correlation

Bonneau, Roland,Liu, Michael T. H.,Lapouyade, Rene

, p. 1547 - 1548 (1989)

Cycloaddition of pyridinium ylides to α-chloroacrylonitrile give indolizines: the regioselectivity of the reaction can be rationalized in terms of nucleophilic attack by the ylides on the olefin.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 115732-59-7