16644-12-5 Usage
Classification
Secondary alcohol This compound is classified as a secondary alcohol, meaning the hydroxyl (OH) group is attached to a carbon atom which is bonded to two other carbon atoms.
Family
Phenethyl alcohol 2-(4-methoxyphenyl)-1-phenylpropan-1-ol belongs to the phenethyl alcohol family, which includes compounds with a phenyl group attached to an ethyl alcohol chain.
Synthesis
Pharmaceutical synthesis and intermediate production This compound is commonly used in the synthesis of pharmaceuticals and as an intermediate in the production of other organic compounds.
Pharmacological properties
Serotonin reuptake and anti-inflammatory potential 2-(4-methoxyphenyl)-1-phenylpropan-1-ol has been studied for its potential pharmacological properties, including its ability to affect serotonin reuptake and its potential use as an anti-inflammatory agent.
Safety precautions
Handle with care Due to potential adverse effects, 2-(4-methoxyphenyl)-1-phenylpropan-1-ol should be handled and used with proper care and management.
Check Digit Verification of cas no
The CAS Registry Mumber 16644-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,4 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16644-12:
(7*1)+(6*6)+(5*6)+(4*4)+(3*4)+(2*1)+(1*2)=105
105 % 10 = 5
So 16644-12-5 is a valid CAS Registry Number.
16644-12-5Relevant articles and documents
Diastereoselective and Enantioselective Conjunctive Cross-Coupling Enabled by Boron Ligand Design
Myhill, Jesse A.,Wilhelmsen, Christopher A.,Zhang, Liang,Morken, James P.
, p. 15181 - 15185 (2018/11/30)
Enantio- and diastereoselective conjunctive cross-coupling of β-substituted alkenylboron "ate" complexes is studied. Whereas β-substitution shifts the chemoselectivity of the catalytic reaction in favor of the Suzuki-Miyaura product, use of a boronic este
