160889-18-9 Usage
Uses
Used in Organic Synthesis:
Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate is used as a building block in organic synthesis for the creation of more complex molecules. Its diverse functional groups facilitate various chemical reactions, making it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Biochemistry Research:
Due to its unique structure and functional groups, Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate is used in biochemical research to explore its potential interactions with biological systems. It may serve as a probe for understanding enzyme mechanisms, receptor binding, or as a precursor to bioactive molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate is used as a starting material for the development of new drugs. Its structural features may confer specific pharmacological properties, making it a candidate for further optimization and investigation as a potential therapeutic agent.
Used in Chemical Intermediates:
Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate is utilized as a chemical intermediate in the production of various specialty chemicals. Its ability to participate in a range of chemical transformations makes it valuable for the synthesis of dyes, fragrances, and other精细化工 products.
Check Digit Verification of cas no
The CAS Registry Mumber 160889-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,8,8 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 160889-18:
(8*1)+(7*6)+(6*0)+(5*8)+(4*8)+(3*9)+(2*1)+(1*8)=159
159 % 10 = 9
So 160889-18-9 is a valid CAS Registry Number.
160889-18-9Relevant articles and documents
PHENYL SUBSTITUTED PYRAZINOYLGUANIDINE SODIUM CHANNEL BLOCKERS POSSESSING BETA AGONIST ACTIVITY
-
, (2008/06/13)
The present invention relates to sodium channel blockers. The present invention also includes a variety of methods of treatment using these inventive sodium channel blockers.
Enantioselective synthesis of salmeterol via asymmetric borane reduction
Hett, Robert,Stare, Ragnar,Helquist, Paul
, p. 9375 - 9378 (2007/10/02)
Enantioselective syntheses of both enantiomers of salmeterol are accomplished using asymmetric borane reductions with chiral oxazaborolidines as catalysts.