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2-Phenyl-4H-1,3-benzodioxine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 43186-35-2 Structure
  • Basic information

    1. Product Name: 2-Phenyl-4H-1,3-benzodioxine
    2. Synonyms: 2-Phenyl-4H-1,3-benzodioxine;2-Phenyl-4H-1,3-benzodioxin
    3. CAS NO:43186-35-2
    4. Molecular Formula: C14H12O2
    5. Molecular Weight: 212.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 43186-35-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Phenyl-4H-1,3-benzodioxine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Phenyl-4H-1,3-benzodioxine(43186-35-2)
    11. EPA Substance Registry System: 2-Phenyl-4H-1,3-benzodioxine(43186-35-2)
  • 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: 43186-35-2(Hazardous Substances Data)

43186-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 43186-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,8 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 43186-35:
(7*4)+(6*3)+(5*1)+(4*8)+(3*6)+(2*3)+(1*5)=112
112 % 10 = 2
So 43186-35-2 is a valid CAS Registry Number.

43186-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-4H-1,3-benzodioxine

1.2 Other means of identification

Product number -
Other names 2-Phenyl-1,3-benzodioxan

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:43186-35-2 SDS

43186-35-2Relevant articles and documents

Reductive openings of acetals: Explanation of regioselectivity in borane reductions by mechanistic studies

Johnsson, Richard,Olsson, Dan,Ellervik, Ulf

, p. 5226 - 5232 (2008/12/21)

(Graph Presented) The mechanisms of regioselective reductive openings of acetals were investigated in several model systems by a combination of Hammett plots, kinetic experiments, density functional calculations, and 11B NMR. The regioselectivity of borane reductions of cyclic acetals can be controlled by the choice of borane. Lewis acid activation of BH3·NMe 3 increases the reaction rate and renders the borane the most electrophilic species, which associates to the more electron-rich oxygen of the acetal. In contrary, without activation, the regioselectivity is instead directed by the Lewis acid, as exemplified by the reaction with BH 3·THF.

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