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| | BOC-TOTA Basic information |
| Product Name: | BOC-TOTA | | Synonyms: | 1-(T-BUTYLOXYCARBONYL-AMINO)-4,7,10-TRIOXA-13-TRIDECANAMINE;1-(TERT-BUTYLOXYCARBONYL-AMINO)-4,7,10-TRIOXA-13-TRIDECANAMINE;3-[2-(2-(3-(BOC-AMINO)PROPYLOXY)ETHOXY)ETHOXY]PROPYLAMINE;BOC-TOTA;BOC-1-AMINO-4,7,10-TRIOXA-13-TRIDECANAMINE;N-Boc-4,7,10-trioxa-1,13-tridecanediamine >=95.0% (NT);tert-butyl N-[3-[2-[2-(3-aminopropoxy)ethoxy]ethoxy]propyl]carbamate;tert-Butyl (3-(2-(2-(3-aminopropoxy)ethoxy) 194920-62-2 | | CAS: | 194920-62-2 | | MF: | C15H32N2O5 | | MW: | 320.42 | | EINECS: | | | Product Categories: | peg | | Mol File: | 194920-62-2.mol |  |
| | BOC-TOTA Chemical Properties |
| Boiling point | 432.4±35.0 °C(Predicted) | | density | 1.035 g/mL at 20 °C | | storage temp. | 2-8°C | | solubility | Chloroform, Ethyl Acetate (Slightly) | | pka | 12.66±0.46(Predicted) | | form | Oil | | color | Colourless |
| WGK Germany | 3 | | F | 10-34 | | HS Code | 2924190090 |
| | BOC-TOTA Usage And Synthesis |
| Description | Boc-TOTA is a linker containing an amino group with a Boc-protected amino group. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine. | | Uses | tert-Butyl (3-(2-(2-(3-Aminopropoxy)ethoxy)ethoxy)propyl)carbamate is used as a reactant in the synthesis of gallium-labeled PET imaging agents for CXCR4 for potential cancer diagnosis. | | Uses | Protected linker. |
| | BOC-TOTA Preparation Products And Raw materials |
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