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CAS

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89539-08-2

1,3-Dioxane, 2-(1-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89539-08-2 Structure

  • Basic information

    1. Product Name: 1,3-Dioxane, 2-(1-phenylethyl)-
    2. Synonyms:
    3. CAS NO:89539-08-2
    4. Molecular Formula: C12H16O2
    5. Molecular Weight: 192.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89539-08-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,3-Dioxane, 2-(1-phenylethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Dioxane, 2-(1-phenylethyl)-(89539-08-2)
    11. EPA Substance Registry System: 1,3-Dioxane, 2-(1-phenylethyl)-(89539-08-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 89539-08-2(Hazardous Substances Data)

89539-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89539-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,3 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89539-08:
(7*8)+(6*9)+(5*5)+(4*3)+(3*9)+(2*0)+(1*8)=182
182 % 10 = 2
So 89539-08-2 is a valid CAS Registry Number.

89539-08-2SDS

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-(1-phenylethyl)-1,3-dioxane

1.2 Other means of identification

Product number -
Other names 2-phenylpropanal trimethylene 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:89539-08-2 SDS

89539-08-2Relevant articles and documents

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

, p. 131 - 135 (2009)

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.

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.

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

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