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5,5-dimethyl-2-(naphthalen-2-yl)-1,3-dioxane is an organic compound characterized by a unique molecular structure. It features a 1,3-dioxane ring, which is a six-membered ring containing two oxygen atoms, and two methyl groups attached to the carbon atoms at positions 5 and 5. The naphthalen-2-yl group is attached to the 2-position of the dioxane ring, providing a significant extension to the molecule's structure. 5,5-dimethyl-2-(naphthalen-2-yl)-1,3-dioxane is known for its potential applications in various chemical and pharmaceutical industries, particularly as a synthetic intermediate or a component in complex organic molecules. Its specific properties, such as solubility and reactivity, can be influenced by the presence of the naphthalene moiety and the methyl groups, making it a compound of interest for further research and development in the field of organic chemistry.

31053-74-4

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31053-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31053-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,5 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31053-74:
(7*3)+(6*1)+(5*0)+(4*5)+(3*3)+(2*7)+(1*4)=74
74 % 10 = 4
So 31053-74-4 is a valid CAS Registry Number.

31053-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-dimethyl-2-naphthalen-2-yl-1,3-dioxane

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

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More Details:31053-74-4 SDS

31053-74-4Downstream Products

31053-74-4Relevant academic research and scientific papers

Efficient and chemoselective acetalization and thioacetalization of carbonyls and subsequent deprotection using InF3 as a reusable catalyst

Madabhushi, Sridhar,Mallu, Kishore Kumar Reddy,Chinthala, Narsaiah,Beeram, China Ramanaiah,Vangipuram, Venkata Sairam

experimental part, p. 697 - 701 (2012/02/15)

An efficient and chemoselective method for preparation of acetals and dithioacetals of aldehydes and their deprotection under catalysis of InF 3 is described.

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