66888-79-7 Usage
Structure
A biphenyl derivative with two hydroxymethyl groups attached to the 2 and 3 positions of the biphenyl ring
Usage
Mainly used as a monomer in the production of high-performance polymers and copolymers
Additional applications
Can be used as a building block in the synthesis of various organic compounds
Potential applications
Pharmaceutical, electronics, and material science industries due to its unique chemical structure and properties
Chemical properties
Unknown, but likely includes reactivity with other compounds to form polymers and copolymers
Physical properties
Unknown, but likely includes a solid state at room temperature based on its molecular weight and structure
Safety
Unknown, but should be handled with care due to its potential reactivity and use in various industries
Environmental impact
Unknown, but may have an impact on the environment due to its use in various industries and potential release into the environment during production or disposal.
Check Digit Verification of cas no
The CAS Registry Mumber 66888-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,8 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66888-79:
(7*6)+(6*6)+(5*8)+(4*8)+(3*8)+(2*7)+(1*9)=197
197 % 10 = 7
So 66888-79-7 is a valid CAS Registry Number.
66888-79-7Relevant academic research and scientific papers
IMMUNE CHECKPOINT INHIBITORS, COMPOSITIONS AND METHODS THEREOF
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Paragraph 0224, (2018/03/25)
The present invention provides synthesis, pharmaceutically acceptable formulations and uses of compounds in accordance with Formula (I), or a stereoisomer, a tautomer or a pharmaceutically acceptable salt thereof. For Formula (I) compounds R1, R2, X1, Y1 and n are as defined in the specification. The inventive Formula (I) compounds are inhibitors of the PD-1/PD-L1 protein/protein binding or functional interaction and find utility in any number of therapeutic applications, including but not limited to treatment of proliferative disorders such as cancer and infectious diseases.
An efficient continuous flow approach to furnish furan-based biaryls
Trinh, Trieu N.,Hizartzidis, Lacey,Lin, Andrew J. S.,Harman, David G.,McCluskey, Adam,Gordon, Christopher P.
, p. 9562 - 9571 (2015/02/19)
Suzuki cross-couplings of 5-formyl-2-furanylboronic acid with activated or neutral aryl bromides were performed under continuous flow conditions in the presence of (Bu)4N+F- and the immobilised t-butyl based palladium cata
