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5663-34-3

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5663-34-3 Usage

General Description

2-(2-phenylethenyl)-1,3-dioxane is a chemical compound with the molecular formula C12H14O2. It is a dioxane derivative with a phenylethene group attached to one of the dioxane rings. 2-(2-phenylethenyl)-1,3-dioxane is used in organic synthesis and as a reagent in chemical reactions. It may also have potential applications in the pharmaceutical industry and in the development of new materials. However, as with any chemical compound, proper handling and safety precautions should be taken when working with 2-(2-phenylethenyl)-1,3-dioxane to minimize the risk of exposure and ensure safe use.

Check Digit Verification of cas no

The CAS Registry Mumber 5663-34-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5663-34:
(6*5)+(5*6)+(4*6)+(3*3)+(2*3)+(1*4)=103
103 % 10 = 3
So 5663-34-3 is a valid CAS Registry Number.

5663-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(Z)-2-phenylethenyl]-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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5663-34-3 SDS

5663-34-3Relevant articles and documents

Acetalization of carbonyl compounds catalyzed by bismuth triflate under solvent-free conditions

Aliyan, Hamid,Fazaeli, Razieh,Massah, Ahmad Reza,Momeni, Ahmad Reza,Naghash, Hamid Javaherian,Moeinifard, Behzad

experimental part, p. 873 - 876 (2012/04/05)

Carbonyl compounds were converted to the corresponding 1,3-dioxolanes and 1,3-dioxanes with ethylene glycol and 1,3-propandiol in the presence of bismuth triflate under solvent-free conditions. In addition, high chemoselective protection of aldehydes in the presence of ketones has been achieved.

Highly efficient and chemoselective acetalization of carbonyl compounds catalyzed by new and reusab e zirconyl triflate, zr0(0tf)2

Moghadam, Majid,Mohammadpoor-Baltork, Iraj,Tangestaninejad, Shahram,Mirkhani, Valiollah,Yazdani, Parvin,Ghorjipoor, Saeedeh

experimental part, p. 131 - 135 (2009/09/30)

Various types of aromatic aldehydes were efficiently converted to their corresponding 1,3-dioxanes and 1,3-dioxolane with 1,3-propanediol and ethylene glycol, respectively, in the presence of catalytic amount of ZrO(OTf) 2 in acetonitrile at room temperature. The catalyst can be reused several times without loss of its catalytic activity. Very short reaction times, selective acetalization of aromatic aldehydes in the presence of aliphatic aldehydes and ketones, very mild reaction conditions, reusability of the catalyst, and easy workup are noteworthy advantages of this method.

Iodine-catalyzed, efficient and mild procedure for highly chemoselective acetalization of carbonyl compounds under neutral aprotic conditions

Karimi, Babak,Golshani, Behzad

, p. 784 - 788 (2007/10/03)

Various types of carbonyl compounds are efficiently converted to their 1,3-dioxanes by the use of 1,3-bis(trimethylsiloxy)propane (BTSP) and a catalytic amount of iodine (3-7 mol%) under essentially neutral aprotic condition.

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