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4-Methoxyphenyl dimethyl phosphate is an organophosphorus compound with the chemical formula C9H13O5P. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 236.17 g/mol. 4-methoxyphenyl dimethyl phosphate is primarily used as an intermediate in the synthesis of various pesticides and pharmaceuticals, particularly in the production of insecticides and herbicides. It is also known for its potential use as a flame retardant and plasticizer. Due to its reactivity and potential health risks, it is important to handle 4-methoxyphenyl dimethyl phosphate with care, following proper safety protocols.

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  • 7357-14-4 Structure
  • Basic information

    1. Product Name: 4-methoxyphenyl dimethyl phosphate
    2. Synonyms: 4-Methoxyphenyl dimethyl phosphate; Phosphoric acid, 4-methoxyphenyl dimethyl ester
    3. CAS NO:7357-14-4
    4. Molecular Formula: C9H13O5P
    5. Molecular Weight: 232.1703
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7357-14-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 275.6°C at 760 mmHg
    3. Flash Point: 134.4°C
    4. Appearance: N/A
    5. Density: 1.216g/cm3
    6. Vapor Pressure: 0.00849mmHg at 25°C
    7. Refractive Index: 1.484
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-methoxyphenyl dimethyl phosphate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-methoxyphenyl dimethyl phosphate(7357-14-4)
    12. EPA Substance Registry System: 4-methoxyphenyl dimethyl phosphate(7357-14-4)
  • 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: 7357-14-4(Hazardous Substances Data)

7357-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7357-14-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7357-14:
(6*7)+(5*3)+(4*5)+(3*7)+(2*1)+(1*4)=104
104 % 10 = 4
So 7357-14-4 is a valid CAS Registry Number.

7357-14-4SDS

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 (4-methoxyphenyl) dimethyl phosphate

1.2 Other means of identification

Product number -
Other names p-methoxyphenyl dimethyl phosphate

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:7357-14-4 SDS

7357-14-4Relevant articles and documents

Semiquantitative Determination of Quinonoid Structures in Isolated Lignins by 31P Nuclear Magnetic Resonance

Argyropoulos, Dimitris S.,Zhang, Liming

, p. 4628 - 4634 (2007/10/03)

A semiquantitative analytical method has been developed for the determination of the total quinonoid content (o-benzoquinones and p-benzoquinones) of soluble lignins. The method is based on detailed measurements and observations made with model o- and p-quinones, which in dry organic solvents were shown to form adducts with trimethyl phosphite in quantitative yield. These adducts gave 31P NMR signals for o- and p-quinones at around -46 and -2 ppm, respectively. In the presence of moisture and lignin the adducts from o-quinones were shown to be hydrolyzed to the open ring product, dimethylphenyl phosphate (-2 ppm), at an overall yield of ~70%. Similarly, the hydrolysis yields of p-quinone adducts with trimethyl phosphite were ~70%. Consequently, a number of important issues in relation to the use of trimethyl phosphite toward the quantitative analysis of quinonoid groups in lignins have been investigated, which permitted the development of an experimental semiquantitative protocol recommended for spectral acquisition.

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