831172-00-0 Usage
Uses
Used in Organic Synthesis:
Carbamic acid, [(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-, 1,1-dimethylethyl ester is used as a reagent in organic synthesis for the preparation of various organic compounds.
Used as a Protecting Group in Organic Chemistry:
Carbamic acid, [(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-, 1,1-dimethylethyl ester is used as a protecting group for hydroxyl groups in organic chemistry reactions, allowing chemists to temporarily block the reactivity of hydroxyl groups during the synthesis process.
Used as a Pharmaceutical Intermediate:
Carbamic acid, [(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-, 1,1-dimethylethyl ester is used as a pharmaceutical intermediate in the development of new drugs.
Used in the Production of Fine Chemicals:
Carbamic acid, [(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-, 1,1-dimethylethyl ester is used in the production of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, agriculture, and materials science.
Used in Pharmaceutical Research:
Carbamic acid, [(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-, 1,1-dimethylethyl ester has been studied for its potential pharmacological properties, particularly as an anti-inflammatory and anti-cancer agent, making it a promising candidate for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 831172-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,1,1,7 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 831172-00:
(8*8)+(7*3)+(6*1)+(5*1)+(4*7)+(3*2)+(2*0)+(1*0)=130
130 % 10 = 0
So 831172-00-0 is a valid CAS Registry Number.
831172-00-0Relevant academic research and scientific papers
Enantiomers of adrenaline-type amino alcohols by Burkholderia cepacia lipase-catalyzed asymmetric acylation
Lundell, Katri,Katainen, Erja,Kiviniemi, Anu,Kanerva, Liisa T.
, p. 3723 - 3729 (2007/10/03)
The enantiomers of norphenylephrine and octopamine were prepared using lipase PS-catalyzed enantioselective acylation with butanoic anhydride. Burkholderia cepacia lipase-catalyzed acylation with butanoic anhydride was used for the preparation of pharmaceutically important norphenylephrine and octopamine enantiomers, all in 98% ee. Reactivity of the phenolic OH groups and easy racemization, especially in the case of octopamine, complicated optimization. For norphenylephrine, chemical N-acylation was fast and allowed the subsequent enzymatic benzylic acylation in situ. The preparation of the octopamine enantiomers became possible by using the N-Fmoc protected substrate and by the Candida antarctica lipase B-catalyzed deprotection of the OH groups before the N-deprotection was performed.
