105229-41-2 Usage
Description
3-Hydroxy-N-[(phenylMethoxy)carbonyl]-O-(phenylMethyl)-L-tyrosine Methyl Ester is a complex organic compound with a chemical structure that features a phenylmethoxycarbonyl group, a phenylmethyl group, and a methyl ester group attached to a modified tyrosine molecule. It is characterized by its yellow sticky oil appearance and is known for its role as an intermediate in the synthesis of L-DOPA metabolites.
Uses
Used in Pharmaceutical Industry:
3-Hydroxy-N-[(phenylMethoxy)carbonyl]-O-(phenylMethyl)-L-tyrosine Methyl Ester is used as an intermediate in the preparation of L-DOPA metabolites for the pharmaceutical industry. Its role in the synthesis process is crucial for the development of medications targeting various medical conditions, particularly those related to the central nervous system.
Used in Chemical Research:
As a complex organic molecule, 3-Hydroxy-N-[(phenylMethoxy)carbonyl]-O-(phenylMethyl)-L-tyrosine Methyl Ester is also utilized in chemical research for studying the properties and reactivity of its constituent groups. This research can lead to the discovery of new applications and improvements in existing synthetic methods.
Used in Material Science:
The unique chemical structure of 3-Hydroxy-N-[(phenylMethoxy)carbonyl]-O-(phenylMethyl)-L-tyrosine Methyl Ester may also find applications in material science, where its properties can be exploited to develop new materials with specific characteristics, such as improved stability or enhanced reactivity in certain conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 105229-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,2 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105229-41:
(8*1)+(7*0)+(6*5)+(5*2)+(4*2)+(3*9)+(2*4)+(1*1)=92
92 % 10 = 2
So 105229-41-2 is a valid CAS Registry Number.
105229-41-2Relevant articles and documents
Benzylic Hydroperoxide Rearrangement: Observations on a Viable and Convenient Alternative to the Baeyer-Villiger Rearrangement
Boger, Dale L.,Coleman, Robert S.
, p. 5436 - 5439 (1986)
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Preparation of selectively protected L-dopa derivatives: Oxidation of tyrosine-3-boronates
Hunter, Luke,Hutton, Craig A.
, p. 1095 - 1098 (2007/10/03)
Conversion of 3-iodo-L-tyrosine to protected tyrosine-3-boronate esters, followed by oxidation with hydrogen peroxide, provides a mild and efficient method for the preparation of selectively protected L-dopa derivatives.
Selectively Protected L-Dopa Derivatives: Application of the Benzylic Hydroperoxide Rearrangement
Boger, Dale L.,Yohannes, Daniel
, p. 5283 - 5286 (2007/10/02)
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