(S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester is a complex organic compound featuring a methyl ester group, an amino group, a carbonyl group, and a phenyl group. It also includes a tert-Butoxycarbonyl (Boc) protecting group, which is frequently utilized in organic synthesis to shield an amine group. (S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester's intricate structure and multiple functional groups suggest potential applications in pharmaceutical research and drug development. Furthermore, its stereochemistry and chirality imply that it may possess specific biological activity or binding properties, making it a compound of interest in the field of medicinal chemistry.
100573-79-3
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Basic information
- Product Name: (S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester
- Synonyms:
- CAS NO:100573-79-3
- Molecular Formula:
- Molecular Weight: 507.627
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester(CAS DataBase Reference)
- NIST Chemistry Reference: (S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester(100573-79-3)
- EPA Substance Registry System: (S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester(100573-79-3)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 100573-79-3(Hazardous Substances Data)
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100573-79-3 Usage
Uses
Used in Pharmaceutical Research:(S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester is used as a research compound for its potential role in the development of new pharmaceuticals. (S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester's structural features and functional groups make it a promising candidate for exploring novel drug interactions and mechanisms.
Used in Drug Development:
In the drug development industry, (S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester is used as a lead compound for designing and synthesizing new therapeutic agents. Its unique structure and functional groups can be leveraged to create drugs with improved efficacy, selectivity, and reduced side effects.
Used in Medicinal Chemistry:
(S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester is utilized as a key intermediate in the synthesis of complex molecules with potential medicinal properties. Its stereochemistry and chirality may provide insights into the compound's specific biological activity, making it a valuable tool in the field of medicinal chemistry.
Used in Chiral Chemistry:
In the field of chiral chemistry, (S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester is used as a model compound to study the effects of stereochemistry on biological activity and drug interactions. Understanding these effects can lead to the development of more effective and safer chiral drugs.
Used in Organic Synthesis:
(S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester serves as a versatile building block in organic synthesis, particularly for the creation of complex molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 100573-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,7 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.Calculate Digit Verification of CAS Registry Number 100573-79:
(8*1)+(7*0)+(6*0)+(5*5)+(4*7)+(3*3)+(2*7)+(1*9)=93
93 % 10 = 3
So 100573-79-3 is a valid CAS Registry Number.
100573-79-3Upstream product
100573-79-3Downstream Products
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(S)-6-tert-Butoxycarbonylamino-2-[(R)-1-((R)-1-ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-ethylamino]-hexanoic acid methyl ester
