109467-74-5 Usage
Description
Phosphoric acid, 1-cyclohexen-1-yl diphenyl ester is a chemical compound that serves as a plasticizer in the production of polyvinyl chloride (PVC) and other polymers. It is a clear, colorless liquid with a faint odor and is insoluble in water.
Uses
Used in Plastics and Polymers Industry:
Phosphoric acid, 1-cyclohexen-1-yl diphenyl ester is used as a plasticizer for enhancing the flexibility, durability, and tensile strength of plastic and rubber materials. It is particularly utilized in the manufacturing of flexible PVC products such as cables, flooring, and tubing, as well as in the production of synthetic rubbers.
Precautions:
Exposure to Phosphoric acid, 1-cyclohexen-1-yl diphenyl ester can be harmful, causing irritation to the skin, eyes, and respiratory system. In high concentrations, it can be toxic if ingested or inhaled. Therefore, proper handling and protective measures are necessary when working with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 109467-74-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,6 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109467-74:
(8*1)+(7*0)+(6*9)+(5*4)+(4*6)+(3*7)+(2*7)+(1*4)=145
145 % 10 = 5
So 109467-74-5 is a valid CAS Registry Number.
109467-74-5Relevant articles and documents
Palladium-catalyzed cross coupling of Grignard reagents with in situ-derived enol phosphates
Miller, Joseph A.
, p. 7111 - 7114 (2002)
A useful, one-pot protocol has been developed for the conversion of enolizable ketones to alkylated or arylated olefins by Pd-catalyzed cross coupling of in situ-generated enol phosphate intermediates with Grignard reagents.
Nickel-catalyzed cross-couplings of cyclohexenyl phosphate and arylboronic acids
Nan, Yang,Yang, Zhen
, p. 3321 - 3324 (2007/10/03)
The Nickel-catalyzed cross-coupling reaction of cyclohexenylphosphate with a variety of arylboronic acids is described here for the first time. This methodology opens the door to other palladium or nickel-catalyzed coupling reactions involving vinyl phosphates.
