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1-diphenoxyphosphoryloxy-3-methyl-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69500-28-3

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69500-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69500-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,0 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69500-28:
(7*6)+(6*9)+(5*5)+(4*0)+(3*0)+(2*2)+(1*8)=133
133 % 10 = 3
So 69500-28-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H17O4P/c1-16-9-8-14-19(15-16)23-24(20,21-17-10-4-2-5-11-17)22-18-12-6-3-7-13-18/h2-15H,1H3

69500-28-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methylphenyl) diphenyl phosphate

1.2 Other means of identification

Product number -
Other names Phosphoric acid,3-methylphenyl diphenyl ester

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:69500-28-3 SDS

69500-28-3Downstream Products

69500-28-3Relevant academic research and scientific papers

Preparation method of cresyl diphenyl phosphate

-

Paragraph 0037; 0049; 0051-0053; 0054; 0065-0068, (2019/11/21)

The invention relates to a preparation method of cresyl diphenyl phosphate. The method includes the steps of: 1) esterification reaction: mixing phosphorus oxychloride with a catalyst, then adding phenol dropwise, and at the end of the reaction, conducting reduced pressure distillation to obtain diphenoxy phosphoryl chloride; 2) reduced pressure reaction: reacting the intermediate diphenoxy phosphoryl chloride obtain in step 1) with m, p-cresol under a reduced pressure, and removing the reacted hydrogen chloride gas to obtain a cresyl diphenyl phosphate crude product; and 3) refining: carryingout alkali washing, washing and reduced pressure distillation on the cresyl diphenyl phosphate crude product obtained in step 2) to obtain cresyl diphenyl phosphate. Phosphorus oxychloride and phenolare employed for reaction to prepare the diphenoxy phosphoryl chloride intermediate, the generated intermediate reacts with m, p-cresol to prepare the product, the synthetic route reduces the impurities phenyl xylylphosphate, tricresyl phosphate and triphenyl phosphate, thus improving the purity.

Synthesis of Unsymmetrical Triaryl Phosphates under Phase-Transfer Catalysis

Genkina,Shipov,Mastryukova,Kabachnik

, p. 1742 - 1744 (2007/10/03)

A Convenient general method for preparing of unsymmetrical triaryl phosphates is elaborated. The influence of the reaction conditions on the yield and purity of the target products is revealed.

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