N-TERT-BUTOXYCARBONYL-D-THREONINE
Boc-D-Thr-OH
CAS: 55674-67-4
Molecular Formula: C9H17NO5
N-TERT-BUTOXYCARBONYL-D-THREONINE - Names and Identifiers
| Name | Boc-D-Thr-OH |
| Synonyms | BOC-D-THR BOC-D-THR-OH Boc-D-Thr-OH Boc-D-threonine BOC-D-THREONINE N-ALPHA-T-BOC-D-THREONINE N-TERT-BUTOXYCARBONYL-D-THREONINE N-(tert-butoxycarbonyl)-D-threonine N-ALPHA-T-BUTOXYCARBONYL-D-THREONINE N-ALPHA-TERT-BUTOXYCARBONYL-D-THREONINE N-(tert-butoxycarbonyl)-D-allothreonine |
| CAS | 55674-67-4 |
| InChI | InChI=1/C9H17NO5/c1-5(11)6(7(12)13)10-8(14)15-9(2,3)4/h5-6,11H,1-4H3,(H,10,14)(H,12,13)/t5-,6-/m1/s1 |
N-TERT-BUTOXYCARBONYL-D-THREONINE - Physico-chemical Properties
| Molecular Formula | C9H17NO5 |
| Molar Mass | 219.24 |
| Density | 1.202g/cm3 |
| Melting Point | 81 °C |
| Boling Point | 387.1°C at 760 mmHg |
| Flash Point | 187.9°C |
| Water Solubility | Slightly soluble in water. |
| Vapor Presure | 1.36E-07mmHg at 25°C |
| Appearance | White crystalline powder |
| Color | White to Almost white |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 9 ° (C=1, AcOH) |
| MDL | MFCD00037807 |
N-TERT-BUTOXYCARBONYL-D-THREONINE - Risk and Safety
| HS Code | 29225090 |
N-TERT-BUTOXYCARBONYL-D-THREONINE - Introduction
Boc-D-Thr-OH(Boc-D-Thr-OH) is an organic compound whose chemical formula is C13H25NO5. It is a compound containing the amino acid threonine, which is weakly acidic under alkaline conditions.
Boc-D-Thr-OH protecting groups and intermediates commonly used in drug development and chemical synthesis. As a protecting group, it can protect the amino group of phenylpropylamino (benzylamine) or threonine, thereby preventing it from reacting with other reagents. As a synthetic intermediate, it can participate in a variety of synthetic reactions such as chain extension and interspersed reactions to build more complex organic molecules.
The method of preparing Boc-D-Thr-OH is generally through the acidolysis reaction of the reaction Boc-D-Thr-O-tbutyl ester with hydrochloric acid (HCl) or some other acid to obtain Boc-D-Thr-OH.
With regard to safety information, Boc-D-Thr-OH are chemicals and appropriate safety measures should be taken. It may irritate the eyes, skin and respiratory system. Wear appropriate protective goggles, gloves and masks during use, and ensure that the operation is carried out in a well-ventilated place. If contact with skin or eyes, rinse immediately with plenty of water and seek medical help. For detailed safety information, consult the safety data sheet of the compound.
Boc-D-Thr-OH protecting groups and intermediates commonly used in drug development and chemical synthesis. As a protecting group, it can protect the amino group of phenylpropylamino (benzylamine) or threonine, thereby preventing it from reacting with other reagents. As a synthetic intermediate, it can participate in a variety of synthetic reactions such as chain extension and interspersed reactions to build more complex organic molecules.
The method of preparing Boc-D-Thr-OH is generally through the acidolysis reaction of the reaction Boc-D-Thr-O-tbutyl ester with hydrochloric acid (HCl) or some other acid to obtain Boc-D-Thr-OH.
With regard to safety information, Boc-D-Thr-OH are chemicals and appropriate safety measures should be taken. It may irritate the eyes, skin and respiratory system. Wear appropriate protective goggles, gloves and masks during use, and ensure that the operation is carried out in a well-ventilated place. If contact with skin or eyes, rinse immediately with plenty of water and seek medical help. For detailed safety information, consult the safety data sheet of the compound.
Last Update：2024-04-09 20:02:46
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CAS: 55674-67-4
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CAS: 55674-67-4
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