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1,3-benzodioxol-5-yl diethyl phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5460-52-6

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5460-52-6 Usage

Synonyms

Ethyl 3,4-methylenedioxybenzene-1-carboxylate

Chemical compound

Yes

Industrial and research purposes

Yes

Physical state

Colorless liquid

Molecular weight

256.2 g/mol

Usage

Flame retardant in plastics, textiles, and electronic products

Usage

Chemical intermediate in synthesis of pharmaceuticals and agrochemicals

Toxicity

Moderately toxic

Potential hazards

Irritation to skin, eyes, and respiratory system

Safety precautions

Necessary when handling the compound

Check Digit Verification of cas no

The CAS Registry Mumber 5460-52-6 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 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5460-52:
(6*5)+(5*4)+(4*6)+(3*0)+(2*5)+(1*2)=86
86 % 10 = 6
So 5460-52-6 is a valid CAS Registry Number.

5460-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-benzodioxol-5-yl diethyl phosphate

1.2 Other means of identification

Product number -
Other names Diaethyl-<3,4-methylendioxy-phenyl>-phosphat

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:5460-52-6 SDS

5460-52-6Downstream Products

5460-52-6Relevant academic research and scientific papers

METAL-FREE DIRECT ARYLATION OF DIALKYL PHOSPHONATES FOR THE SYNTHESIS OF MIXED ALKYL ARYL PHOSPHONATES

-

Paragraph 00385; 00402; 00442, (2019/02/15)

Provided herein are phosphates, thiophosphates, phosphonates, and phosphinates, methods of making same, and methods of using these compounds and methods for the generation of pharmaceutically relevant phosphate, phosphonate, and phosphinate analogs. This

Tf2O-Promoted Activating Strategy of Phosphate Analogues: Synthesis of Mixed Phosphates and Phosphinate

Huang, Hai,Ash, Jeffrey,Kang, Jun Yong

supporting information, p. 4938 - 4941 (2018/08/24)

A metal-, toxic chloride reagent-free activating strategy of various phosphates has been developed. This method enables the facile synthesis of functional phosphates such as alkyl phosphates, aza phosphates, thiophosphate, and mixed diaryl phosphates. A transient phosphorylpyridin-1-ium species in situ generated from phosphates with Tf2O/pyridine readily undergoes a substitution reaction with diverse nucleophiles to form versatile phosphate compounds.

Photoinduced three-component reaction: A convenient access to 3-arylacetals or 3-arylketals

Lazzaroni, Simone,Protti, Stefano,Fagnoni, Maurizio,Albini, Angelo

supporting information; experimental part, p. 349 - 352 (2009/08/15)

(Chemical Equation Presented) A mild and versatile method for the photoinduced three-component synthesis of 3-arylacetals and ketals is presented. Desired targets are smoothly obtained by irradiating aromatic halides or esters in alcohols, in the presence

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