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(3R,4S,5S)-4-((tert-butoxycarbonyl)amino)-3-hydroxy-5-methyl-heptanoic acid is a complex organic compound with a heptanoic acid backbone, featuring a hydroxy, methyl, and amino group attached to it. The presence of the tert-butoxycarbonyl group signifies that it is a protected amino acid, which is commonly utilized in peptide synthesis to prevent unwanted reactions. The specific stereochemistry of the compound is denoted by the (3R,4S,5S) configuration, indicating the arrangement of the substituents on the chiral carbon atoms. This unique structure may grant the compound various applications in synthetic chemistry, biochemical research, and pharmaceutical development.

133645-50-8

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133645-50-8 Usage

Uses

Used in Synthetic Chemistry:
(3R,4S,5S)-4-((tert-butoxycarbonyl)amino)-3-hydroxy-5-methyl-heptanoic acid is used as a protected amino acid in synthetic chemistry for peptide synthesis, providing a stable and versatile building block for the creation of complex peptide structures.
Used in Biochemical Research:
In biochemical research, (3R,4S,5S)-4-((tert-butoxycarbonyl)amino)-3-hydroxy-5-methyl-heptanoic acid is used as a chiral compound to study the effects of stereochemistry on biological activity and to develop novel bioactive molecules with potential applications in various fields.
Used in Pharmaceutical Development:
(3R,4S,5S)-4-((tert-butoxycarbonyl)amino)-3-hydroxy-5-methyl-heptanoic acid is used as a key intermediate in the development of new pharmaceuticals, particularly those targeting specific biological pathways or receptors. Its unique structure and stereochemistry may contribute to the design of more effective and selective drugs.
Used in Drug Delivery Systems:
In the pharmaceutical industry, (3R,4S,5S)-4-((tert-butoxycarbonyl)amino)-3-hydroxy-5-methyl-heptanoic acid is used as a component in drug delivery systems, potentially enhancing the bioavailability and targeting of therapeutic agents.
Used in Chiral Catalysts:
(3R,4S,5S)-4-((tert-butoxycarbonyl)amino)-3-hydroxy-5-methyl-heptanoic acid can be used as a chiral catalyst in asymmetric synthesis, facilitating the production of enantiomerically pure compounds with high selectivity and efficiency.
Used in Analytical Chemistry:
In analytical chemistry, (3R,4S,5S)-4-((tert-butoxycarbonyl)amino)-3-hydroxy-5-methyl-heptanoic acid can be employed as a reference compound for the development and validation of analytical methods, such as chiral chromatography and mass spectrometry, to accurately determine the stereochemistry of other compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 133645-50-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,4 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133645-50:
(8*1)+(7*3)+(6*3)+(5*6)+(4*4)+(3*5)+(2*5)+(1*0)=118
118 % 10 = 8
So 133645-50-8 is a valid CAS Registry Number.

133645-50-8Upstream product

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