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92556-46-2

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92556-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92556-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,5 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92556-46:
(7*9)+(6*2)+(5*5)+(4*5)+(3*6)+(2*4)+(1*6)=152
152 % 10 = 2
So 92556-46-2 is a valid CAS Registry Number.

92556-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenyl(propoxy)phosphane

1.2 Other means of identification

Product number -
Other names Propyloxy-diphenyl-phosphin

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:92556-46-2 SDS

92556-46-2Relevant articles and documents

Novel synthesis method of clean and safe photoinitiator (2,4,6-trimethylbenzoyldiphenyl-diphenylphosphine oxide)

-

Paragraph 0049; 0050, (2019/06/12)

The invention relates to the technical field of synthesis of photoinitiators, in particular to a novel synthesis method of a clean and safe photoinitiator (2,4,6-trimethylbenzoyldiphenyl-diphenylphosphine oxide). The method includes the steps of evenly mixing anhydrous alcohol with N-methylimidazole at the room temperature, raising the temperature to 30-50%, controlling the temperature, dropwise adding diphenylphosphine oxide, raising the temperature to 50-100 DEG C, conducting the constant-temperature reaction for 2-3 h, conducting standing and layering to take supernatant liquid for decompressing and distilling to obtain diphenyl alkoxylphosphine, making the diphenyl alkoxylphosphine start to react with 2,4,6-trimethylbenzoyldiphenyl chloride at the controlled temperature of 50 DEG C under the vacuum condition of -0.098 Mpa, raising the temperature by 10 DEG C every 20 minutes until the temperature is raised to 90 DEG C, conducting the constant-temperature reaction for 4-8 h, and adding 50% ethyl alcohol crystals to obtain a target product. The produced byproduct is subjected to vacuum removal and then enters a tail gas recovery system to be recovered through two stages of condensation. The synthesis method is simple in step, safe, clean, low in running cost and high in byproduct recovery rate.

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