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2164-33-2

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2164-33-2 Usage

Description

2-(CHLOROMETHYL)-2,3-DIHYDRO-1,4-BENZODIOXINE is an organic compound characterized by its unique chemical structure, which features a benzodioxine ring with a chloromethyl group attached to the second carbon. This structure endows the compound with specific reactivity and synthetic utility in the field of organic chemistry.

Uses

Used in Pharmaceutical Industry:
2-(CHLOROMETHYL)-2,3-DIHYDRO-1,4-BENZODIOXINE is used as a synthetic intermediate for the production of various pharmaceutical compounds. Its unique structure allows for the creation of a wide range of benzene-based drugs with potential therapeutic applications.
Used in Chemical Synthesis:
2-(CHLOROMETHYL)-2,3-DIHYDRO-1,4-BENZODIOXINE is used as a reactant in the synthesis of various organic compounds, such as benzenesulfonamide derivatives. Its reactivity and versatility make it a valuable building block for the development of new chemical entities with diverse applications.
Used in Research and Development:
In the field of research and development, 2-(CHLOROMETHYL)-2,3-DIHYDRO-1,4-BENZODIOXINE serves as a key compound for exploring new reaction pathways and developing innovative synthetic methods. Its unique properties can be harnessed to design and synthesize novel molecules with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 2164-33-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2164-33:
(6*2)+(5*1)+(4*6)+(3*4)+(2*3)+(1*3)=62
62 % 10 = 2
So 2164-33-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClO2/c10-5-7-6-11-8-3-1-2-4-9(8)12-7/h1-4,7H,5-6H2

2164-33-2 Well-known Company Product Price

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  • Alfa Aesar

  • (L04137)  2-Chloromethyl-1,4-benzodioxane, 97%   

  • 2164-33-2

  • 5g

  • 644.0CNY

  • Detail
  • Alfa Aesar

  • (L04137)  2-Chloromethyl-1,4-benzodioxane, 97%   

  • 2164-33-2

  • 25g

  • 2685.0CNY

  • Detail

2164-33-2SDS

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-(chloromethyl)-2,3-dihydro-1,4-benzodioxine

1.2 Other means of identification

Product number -
Other names 2-chloromethylbenzodioxane(1,4)

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:2164-33-2 SDS

2164-33-2Relevant articles and documents

A sulfuric acid guanidine lives synthesis method

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Paragraph 0026; 0027; 0034; 0035, (2017/08/26)

The invention belongs to the technical field of organic drug synthesis, and particularly relates to a guanoxan sulfate synthesis method. The method comprises steps as follows: 1), 2-hydroxymethyl-1,4-benzodioxane and thionyl chloride have a chlorination reaction under the condition of existence of a solvent I, and 2-chloromethyl-1,4-benzodioxane is obtained; 2), 2-chloromethyl-1,4-benzodioxane and guanidine are condensed under the condition of existence of alkali and a solvent II, guanoxan is obtained, guanoxan and sulfuric acid are salified, and a finished product guanoxan sulfate is obtained. According to the guanoxan sulfate synthesis method, technological synthesis steps are simple, a route is short, raw material toxicity is relatively lower, and the yield and the purity of the product are high.

Research on the calcium inhibition of a heterocyclic oxygen compound series

Mouysset,Bellan,Payard,Tisne-Versailles

, p. 805 - 813 (2007/10/02)

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Neuroleptic n-oxacyclyl-alkylpiperidine derivatives

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, (2008/06/13)

Neuroleptically active compounds of the formula STR1 wherein R6 and R10 are --H or CH3 ; R7 and R8 are independently --H, --F, --Cl, or --CH3 ; and R9 is --F, --Cl, --CH3, or --OCH3.

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