352545-44-9 Usage
Description
(S)-t-butyl-leucinol; hydrochloride is a chemical compound derived from t-butyl-leucine, a branched-chain amino acid. It is classified as a hydrochloride salt, resulting from the reaction between t-butyl-leucinol and hydrochloric acid. (S)-t-butyl-leucinol; hydrochloride is characterized by its chirality and structural features, making it a promising candidate for pharmaceutical and industrial applications. Its hydrochloride salt form enhances its stability and solubility in water, which could be beneficial for specific processes within these industries.
Uses
Used in Pharmaceutical Industry:
(S)-t-butyl-leucinol; hydrochloride is used as a building block for the production of chiral drugs due to its unique chiral properties. (S)-t-butyl-leucinol; hydrochloride's structural characteristics allow it to be a valuable component in the development of new medications with improved efficacy and selectivity.
Used in Chemical Synthesis:
In the field of chemical synthesis, (S)-t-butyl-leucinol; hydrochloride serves as a chiral auxiliary. Its presence can help control the stereochemistry of reactions, leading to the production of enantiomerically pure compounds. This is particularly important in the synthesis of complex molecules, such as pharmaceuticals and agrochemicals, where the desired biological activity is often associated with a specific enantiomer.
Further research and development of (S)-t-butyl-leucinol; hydrochloride may reveal additional potential uses and applications for this versatile compound in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 352545-44-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,4 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 352545-44:
(8*3)+(7*5)+(6*2)+(5*5)+(4*4)+(3*5)+(2*4)+(1*4)=139
139 % 10 = 9
So 352545-44-9 is a valid CAS Registry Number.
352545-44-9Relevant articles and documents
Preparation method of N-alkoxy or benzyloxycarbonyl chiral amino acid
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Paragraph 0054-0056, (2018/03/24)
The invention provides a preparation method of N-alkoxy or benzyloxycarbonyl amino acid, particularly provides a preparation method of N-alkoxy or benzyloxycarbonyl chiral amino acid, and more particularly provides a preparation method of N-alkoxy or benzyloxycarbonyl-L-amino acid or N-alkoxy or benzyloxycarbonyl-D-amino acid. In the preparation method, a resolving agent is not required for chemical resolution, and the N-alkoxy or benzyloxycarbonyl chiral amino acid with high optical purity can be prepared. The N-alkoxy or benzyloxycarbonyl chiral amino acid is a very important medicine intermediate. According to the preparation method of the N-alkoxy or benzyloxycarbonyl-L-amino acid, provided by the invention, a reaction formula is as follows in the description, wherein R1 is an alkyl group, preferably a tert-butyl group; R2 is an azido group or an imide group, n is 0 or 1, and m is 1.
