29509-30-6 Usage
Uses
Used in Fragrance and Perfume Industry:
2-Phenoxy-1-phenylpropan-1-ol is used as a key ingredient in the production of fragrances and perfumes for its aromatic properties, enhancing the scent and longevity of these products.
Used in Industrial Manufacturing:
2-Phenoxy-1-phenylpropan-1-ol serves as a chemical intermediate in the manufacturing of various industrial products, contributing to the development of a wide range of consumer and industrial goods.
Used in Medical and Scientific Applications:
2-Phenoxy-1-phenylpropan-1-ol is used as an antimicrobial and antifungal agent in some medical and scientific applications, thanks to its ability to inhibit the growth of certain microorganisms, making it a valuable component in certain treatments and research.
Used in Synthesis of Organic Compounds:
As a chemical intermediate, 2-Phenoxy-1-phenylpropan-1-ol plays a crucial role in the synthesis of other organic compounds, facilitating the creation of new materials and substances with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 29509-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,0 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29509-30:
(7*2)+(6*9)+(5*5)+(4*0)+(3*9)+(2*3)+(1*0)=126
126 % 10 = 6
So 29509-30-6 is a valid CAS Registry Number.
29509-30-6Relevant academic research and scientific papers
Iron-Catalyzed Borrowing Hydrogen β- C(sp3)-Methylation of Alcohols
Polidano, Kurt,Williams, Jonathan M. J.,Morrill, Louis C.
, p. 8575 - 8580 (2019/09/12)
Herein we report the iron-catalyzed β-C(sp3)-methylation of primary alcohols using methanol as a C1 building block. This borrowing hydrogen approach employs a well-defined bench-stable (cyclopentadienone)iron(0) carbonyl complex as precatalyst (5 mol %) and enables a diverse selection of substituted 2-arylethanols to undergo β-C(sp3)-methylation in good isolated yields (24 examples, 65% average yield).
THE INFLUENCE OF α-ARYL ETHERS ON THE ASYMMETRIC REDUCTION OF CARBONYLS
Samuels, William D.,Nelson, David A.,Hallen, Richard T.
, p. 3091 - 3094 (2007/10/02)
The asymmetric reduction of α-aryl ethers 1 was found to be strongly influenced by the presence of ortho substituents on the aryl ring.Groups (methoxy or hydroxy) that chelate metal cations tend to stabilize a "locked" bicyclic 4 which, intermediate when
