89929-93-1 Usage
General Description
[3-(2-FURYL)PHENYL]METHANOL is a chemical compound with a molecular formula C13H12O2. It is also known as 2-(3-hydroxyphenyl)furan and is commonly used as a flavoring ingredient. It is a white crystalline solid that is soluble in organic solvents. [3-(2-FURYL)PHENYL]METHANOL is often used in the production of flavor and fragrance products due to its sweet, nutty, and caramel-like aroma. In addition to its use in the food and beverage industry, [3-(2-FURYL)PHENYL]METHANOL has also been studied for its potential therapeutic applications, including its anti-inflammatory and antioxidant properties. However, further research is needed to fully understand its potential benefits and health impacts.
Check Digit Verification of cas no
The CAS Registry Mumber 89929-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,2 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89929-93:
(7*8)+(6*9)+(5*9)+(4*2)+(3*9)+(2*9)+(1*3)=211
211 % 10 = 1
So 89929-93-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O2/c12-8-9-3-1-4-10(7-9)11-5-2-6-13-11/h1-7,12H,8H2
89929-93-1Relevant articles and documents
Pd-mediated C-C and C-S bond formation on solid support: A scope and limitations study
Wendeborn, Sebastian,Berteina, Sabine,Brill, Wolfgang K.-D.,De Mesmaeker, Alain
, p. 671 - 675 (2007/10/03)
The scope and limitations of Pd(0)-mediated coupling reactions between aromatic halides linked to a polystyrene resin and boronic acid derivatives (Suzuki coupling), aromatic and vinylic tin compounds (Stille coupling), as well as thiols are reported. For all reactions, conditions were optimized and evaluated with various reagents. In many cases, upon cleavage from the solid support, products were obtained in excellent yields. In most cases, the optimized reaction conditions are superior to those previously reported in the literature.
