101402-02-2 Usage
Description
(S)-(4-aminophenyl)(phenyl)methanol, with the molecular formula C13H13NO, is a chemical compound featuring a benzene ring with a hydroxyl group attached to the carbon atom and an amino group at the para position of the benzene ring. This versatile chemical is commonly utilized in chemical research and synthesis, and it holds potential applications in the pharmaceutical and organic chemistry sectors. Careful handling is advised due to its potential hazards if not properly managed.
Uses
Used in Chemical Research and Synthesis:
(S)-(4-aminophenyl)(phenyl)methanol is used as an intermediate in the synthesis of various organic compounds for [application reason] its structural features that allow for further chemical reactions and modifications.
Used in Pharmaceutical Industry:
(S)-(4-aminophenyl)(phenyl)methanol is used as a building block for the development of new pharmaceuticals for [application reason] its potential to be incorporated into drug molecules targeting specific biological pathways.
Used in Organic Chemistry:
(S)-(4-aminophenyl)(phenyl)methanol is used as a reagent in organic chemistry for [application reason] its ability to participate in a range of chemical reactions, contributing to the formation of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 101402-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,4,0 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101402-02:
(8*1)+(7*0)+(6*1)+(5*4)+(4*0)+(3*2)+(2*0)+(1*2)=42
42 % 10 = 2
So 101402-02-2 is a valid CAS Registry Number.
101402-02-2Relevant articles and documents
Enzyme-catalyzed enantioselective diaryl ketone reductions
Truppo, Matthew D.,Pollard, David,Devine, Paul
, p. 335 - 338 (2007)
(Chemical Equation Presented) The synthesis of diarylmethanols via the reduction of a range of substituted benzophenone and benzoylpyridine derivatives with ketoreductase enzymes (KREDs) has afforded chiral products with high yield (>90%) and ee (up to >99%). Ortho, meta, and para substitutions with a variety of electron-donating, electron-withdrawing, and halogen groups were examined. Substitution at the ortho position and/or highly electronically dissymmetric molecules were not required for good selectivity, as is the case with conventional chemical catalyst reductions.
An enantiopure galactose oxidase model: synthesis of chiral amino alcohols through oxidative kinetic resolution catalyzed by a chiral copper complex
Mannam, Sreedevi,Sekar, Govindasamy
, p. 497 - 502 (2009)
An enantiopure galactose oxidase (GO) enzyme model has been synthesized from readily available (R)-BINAM and Cu(OTf)2, and the enantiopure GO model has been effectively used in situ as an efficient chiral catalyst for the synthesis of chiral amino alcohols through oxidative kinetic resolution (OKR), where molecular oxygen is used as the sole oxidant. Under the proposed catalytic conditions, both ortho- and para-substituted amino alcohols were resolved with good to excellent enantiomeric excesses through oxidative kinetic resolution.
