(2S,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-pent-4-enoic acid is a synthetic compound derived from the natural compound 2-amino-3-hydroxy-4-phenylbutyric acid, which has been studied for its anti-cancer and anti-inflammatory properties. The addition of a tert-butoxycarbonyl (Boc) protecting group to the amino group makes it useful for peptide synthesis, as the Boc group can be selectively removed under mild conditions. The presence of a hydroxy and enoic acid group in the molecule also suggests potential reactivity and functionalization for various chemical modifications. Overall, (2S,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-pent-4-enoic acid represents a versatile building block for the development of novel pharmaceuticals and bioactive molecules.
101623-96-5
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Basic information
- Product Name: (2S,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-pent-4-enoic acid
- Synonyms:
- CAS NO:101623-96-5
- Molecular Formula:
- Molecular Weight: 231.249
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 408.5±45.0 °C(Predicted)
- Flash Point: N/A
- Appearance: N/A
- Density: 1.192±0.06 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (2S,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-pent-4-enoic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (2S,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-pent-4-enoic acid(101623-96-5)
- EPA Substance Registry System: (2S,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-pent-4-enoic acid(101623-96-5)
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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: 101623-96-5(Hazardous Substances Data)
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101623-96-5 Usage
Uses
Used in Pharmaceutical Industry:(2S,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-pent-4-enoic acid is used as a building block for the development of novel pharmaceuticals and bioactive molecules due to its potential biological and pharmaceutical applications.
Used in Peptide Synthesis:
(2S,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-pent-4-enoic acid is used as a protected amino acid in peptide synthesis, as the Boc protecting group can be selectively removed under mild conditions, allowing for the incorporation of the compound into peptide sequences.
Check Digit Verification of cas no
The CAS Registry Mumber 101623-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,6,2 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.Calculate Digit Verification of CAS Registry Number 101623-96:
(8*1)+(7*0)+(6*1)+(5*6)+(4*2)+(3*3)+(2*9)+(1*6)=85
85 % 10 = 5
So 101623-96-5 is a valid CAS Registry Number.
101623-96-5Upstream product
101623-96-5Downstream Products
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(2S,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-pent-4-enoic acid
