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2,3-Dihydro-α-methyl-1,4-benzodioxin-2-methanamine is a complex organic compound with the molecular formula C10H13NO2. It is a derivative of benzodioxin, featuring a methyl group attached to the alpha carbon and a methanamine group at the 2-position. 2,3-Dihydro-α-methyl-1,4-benzodioxin-2-methanamine is characterized by its 2,3-dihydro structure, which means it has two hydrogen atoms added to the benzene ring, and a saturated carbon chain attached to the nitrogen atom. It is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound's properties, such as solubility and stability, can vary depending on the specific conditions and its intended use.

2469-18-3

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2469-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2469-18-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2469-18:
(6*2)+(5*4)+(4*6)+(3*9)+(2*1)+(1*8)=93
93 % 10 = 3
So 2469-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-7(11)10-6-12-8-4-2-3-5-9(8)13-10/h2-5,7,10H,6,11H2,1H3

2469-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,3-dihydro-1,4-benzodioxin-3-yl)ethanamine

1.2 Other means of identification

Product number -
Other names 1-(2,3-dihydro-1,4-benzodioxin-2-yl)ethanamine

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:2469-18-3 SDS

2469-18-3Relevant academic research and scientific papers

Silver-Catalyzed Radical Transformation of Aliphatic Carboxylic Acids to Oxime Ethers

Zhu, Yuchao,Wen, Xiaojin,Song, Song,Jiao, Ning

, p. 6465 - 6472 (2016/10/14)

Oximes and oxime ethers are privileged building blocks and can be conveniently converted to ketones, amines, hydroxylamines, and nitriles. We describe the catalytic decarboxylation of aliphatic carboxylic acids to oxime ethers. With AgNO3 as the catalyst, valuable oxime ethers bearing various substituents could be easily obtained. The broad substrate scope, easy accessibility of aliphatic carboxylic acids, and mild reaction conditions make this strategy immediately applicable to the synthesis, late-stage functionalization, and modification of biologically active compounds. Experimental studies show the reaction undergoes a radical process.

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