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2-Benzyl-2-methyl-1,3-dioxane is an organic compound with the molecular formula C11H14O2. It is a cyclic ether that features a benzyl group attached to a 1,3-dioxane ring, which is a six-membered ring containing two oxygen atoms. This chemical is known for its stability and is often used as a synthetic intermediate in the preparation of various pharmaceuticals and agrochemicals. Its structure provides a platform for further functionalization, making it a valuable building block in organic synthesis. The compound is characterized by its unique reactivity and can participate in a range of chemical transformations, such as nucleophilic substitutions and electrophilic additions, due to the presence of the electron-rich benzene ring and the strained dioxane ring.

6413-86-1

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6413-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6413-86-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6413-86:
(6*6)+(5*4)+(4*1)+(3*3)+(2*8)+(1*6)=91
91 % 10 = 1
So 6413-86-1 is a valid CAS Registry Number.

6413-86-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-2-methyl-1,3-dioxane

1.2 Other means of identification

Product number -
Other names 2-Methyl-2-benzyl-1,3-dioxan

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:6413-86-1 SDS

6413-86-1Relevant academic research and scientific papers

2,4,4,6-Tetrabromo-2,5-cyclohexadienone (TABCO) as a versatile, efficient, and chemoselective catalyst for the acetalization and transacetalization of carbonyl compounds, the preparation of acetonides from epoxides and acylals (1,1-diacetates) from aldehydes

Firouzabadi, Habib,Iranpoor, Nasser,Shaterian, Hamid Reza

, p. 2195 - 2205 (2007/10/03)

The efficient and chemoselective preparation of acetals and ketals from carbonyl compounds, transacetalization reactions, the conversion of epoxides to acetonides, and the preparation of acylals from aldehydes in the presence of catalytic amounts of 2,4,4,6-tetrabromo-2,5-cyclohexadienone (TABCO) are described.

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