Welcome to LookChem.com Sign In|Join Free
  • or
2-Benzyl-4-methyl-1,3-dioxolane is a cyclic organic compound characterized by a 1,3-dioxolane ring, which consists of two oxygen atoms and three carbon atoms. The molecule features a benzyl group (C6H5-CH2-) attached to the second carbon atom and a methyl group (-CH3) at the fourth carbon position. This chemical is often used as a synthetic intermediate in the preparation of various pharmaceuticals and fragrances due to its unique structure and reactivity. It is typically synthesized through the reaction of an aldehyde or ketone with an alkylene oxide, followed by intramolecular cyclization. The compound is known for its stability and can be further functionalized to yield a range of valuable products in the chemical industry.

5468-05-3

Post Buying Request

5468-05-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5468-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5468-05-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5468-05:
(6*5)+(5*4)+(4*6)+(3*8)+(2*0)+(1*5)=103
103 % 10 = 3
So 5468-05-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2/c1-9-8-12-11(13-9)7-10-5-3-2-4-6-10/h2-6,9,11H,7-8H2,1H3

5468-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-4-methyl-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names Phenylacetaldehyde propyleneglycol acetal

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:5468-05-3 SDS

5468-05-3Relevant academic research and scientific papers

Iodine-catalyzed tandem synthesis of terminal acetals and glycol mono esters from olefins

Kumar, Macharla Arun,Swamy, Peraka,Naresh, Mameda,Reddy, Marri Mahender,Rohitha, Chozhiyath Nappunni,Prabhakar, Sripadi,Sarma, Akella Venkata Subrahmanya,Kumar, Joseph Richard Prem,Narender, Nama

supporting information, p. 1711 - 1713 (2013/03/14)

A new metal-free protocol is described for the synthesis of terminal acetals by tandem oxidative rearrangement of olefins using oxone as an oxidant in the presence of iodine. Moreover, a one-pot procedure for the preparation of glycol mono esters from olefins is also presented for the first time using the same reagent system. The Royal Society of Chemistry 2013.

Non-acid catalytic acetalisation of aldehydes with diols in ionic liquids

Zhang, Fan,Xu, Dan-Qian,Luo, Shu-Ping,Liu, Bao-You,Du, Xiao-Hua,Xu, Zhen-Yuan

, p. 773 - 774 (2007/10/03)

The acetalisation of aldehydes with diols to corresponding 1,3-dioxolanes has been accomplished using ionic liquids as catalyst and reaction media. In the reaction process the removal of water produced and other catalysts were not necessary. High conversion and good selectivity were obtained when using HMImBF4, which could be easily recycled and reused.

Acetals by AlFe-pillared montmorillonite catalysis

Cramarossa, Maria Rita,Forti, Luca,Ghelfi, Franco

, p. 15889 - 15894 (2007/10/03)

AlFe-pillared montmorillonite is an efficient catalyst for acetals preparation in CH2Cl2 at room temperature.

A Simple and Efficient Conversion of Aldehyde Acetals into Esters

Sugai, Saburo,Kodama, Takashi,Akaboshi, Sanya,Ikegami, Shiro

, p. 99 - 105 (2007/10/02)

The reaction of aldehydic acetals with hypochlorous acid in acetic acid-acetone afforded the corresponding esters in excellent yields.From cyclic acetals, only the corresponding hydroxyalkyl esters were obtained.Keywords - acetal; hypochlorite; hypochlorous acid; conversion; ester; hydroxyalkyl ester; regioselectivity

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5468-05-3