9H-fluoren-9-ylmethyl [(1R,2R)-2-tert-butoxy-1-(hydroxymethyl)propyl]carbamate - Names and Identifiers
Name | FMOC-THR(TBU)-OL
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Synonyms | FMOC-THR(TBU)-OL Fmoc-Thr(OtBu)-Ol N-FMOC-L-THR(TBU)-OL FMOC-O-T-BUTYL-L-THREONINOL N-ALPHA-FMOC-O-T-BUTYL-L-THREONINOL FMOC-(2R,3R)-2-AMINO-3-T-BUTOXY-1-BUTANOL N-FMOC-(2R,3R)-2-AMINO-3-T-BUTOXY-1-BUTANOL N-(9-FLUORENYLMETHOXYCARBONYL)-O-T-BUTYL-L-THREONINOL N-FMOC-L-THR(TBU)-OL-N-FMOC-(2R,3R)-2-AMINO-3-T-BUTOXY-1-BUTANOL N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-O-TERT-BUTYL-L-THREONINOL 9H-fluoren-9-ylmethyl [(1R,2R)-2-tert-butoxy-1-(hydroxymethyl)propyl]carbamate (9H-fluoren-9-yl)methyl N-[(2R,3R)-3-(tert-butoxy)-1-hydroxybutan-2-yl]carbamate
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CAS | 189337-28-8
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InChI | InChI=1/C23H29NO4/c1-15(28-23(2,3)4)21(13-25)24-22(26)27-14-20-18-11-7-5-9-16(18)17-10-6-8-12-19(17)20/h5-12,15,20-21,25H,13-14H2,1-4H3,(H,24,26)/t15-,21-/m1/s1 |
9H-fluoren-9-ylmethyl [(1R,2R)-2-tert-butoxy-1-(hydroxymethyl)propyl]carbamate - Physico-chemical Properties
Molecular Formula | C23H29NO4
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Molar Mass | 383.48 |
Density | 1.144 |
Boling Point | 576.5±45.0 °C(Predicted) |
Flash Point | 302.454°C |
Vapor Presure | 0mmHg at 25°C |
pKa | 11.00±0.46(Predicted) |
Storage Condition | Sealed in dry,2-8°C |
Refractive Index | 1.563 |
MDL | MFCD00235950 |
Physical and Chemical Properties | Storage Conditions: Store at 0 ℃ |
9H-fluoren-9-ylmethyl [(1R,2R)-2-tert-butoxy-1-(hydroxymethyl)propyl]carbamate - Introduction
FMOC-THR(TBU)-OL is an organic compound with the chemical formula C16H23NO3. The following is a description of its nature, use, formulation and safety information:
Nature:
FMOC-THR(TBU)-OL is a solid with a white to yellowish crystalline form. It is very soluble in organic solvents such as methanol, ethanol and dichloromethane.
Use:
FMOC-THR(TBU)-OL is commonly used as a catalyst in organic synthesis reactions. It can be used to synthesize organic compounds such as hydrophobic compounds, amino acids and polypeptides. In addition, it can also be used as a synthetic raw material for pharmaceutical intermediates and biologically active substances.
Method:
The method for preparing FMOC-THR(TBU)-OL can be obtained by reacting an initiating substance with ethyl fluorenecate. The specific synthetic steps can be fine-tuned according to laboratory conditions and desired purity.
Safety Information:
FMOC-THR(TBU)-OL has limited toxicity and hazard data, it is necessary to take appropriate laboratory safety measures when handling and using. During operation, avoid inhalation, ingestion or skin contact. If inhaled or exposed to the compound, wash the affected area immediately and seek medical help if necessary.
Last Update:2024-04-09 20:49:11