BOC-12-ADO-OH manufacturers
- Boc-12-Ado-OH
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- $1980.00
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2026-05-11
- CAS:18934-81-1
- Purity:
- Supply Ability: 10g
- BOC-12-ADO-OH
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2024-10-22
- CAS:18934-81-1
- Min. Order: 1KG
- Purity: 95%~99.99%
- Supply Ability: 10 MT/ Month
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| | BOC-12-ADO-OH Basic information |
| Product Name: | BOC-12-ADO-OH | | Synonyms: | 12-(BOC-AMINO)DODECANOIC ACID;BOC-12-ADO-OH;BOC-12-AMINODODECANOIC ACID;BOC-12-AMINOLAURIC ACID;BOC-NH-(CH2)11-COOH;N-TERT-BUTYLOXYCARBONYL-12-AMINO-DODECANOIC ACID;T-BUTOXYCARBONYL-12-AMINODODECANOIC ACID;T-BUTOXYCARBONYL-12-AMINOLAURIC ACID | | CAS: | 18934-81-1 | | MF: | C17H33NO4 | | MW: | 315.45 | | EINECS: | | | Product Categories: | Amino Acids | | Mol File: | 18934-81-1.mol |  |
| | BOC-12-ADO-OH Chemical Properties |
| Melting point | 83.5-84.5 °C | | Boiling point | 454.5±18.0 °C(Predicted) | | density | 0.997±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,2-8°C | | form | powder | | pka | 4.78±0.10(Predicted) | | color | colorless to white | | BRN | 1980302 | | Major Application | peptide synthesis | | InChI | InChI=1S/C17H33NO4/c1-17(2,3)22-16(21)18-14-12-10-8-6-4-5-7-9-11-13-15(19)20/h4-14H2,1-3H3,(H,18,21)(H,19,20) | | InChIKey | NNPOZNVKUHYVEJ-UHFFFAOYSA-N | | SMILES | C(O)(=O)CCCCCCCCCCCNC(OC(C)(C)C)=O |
| WGK Germany | 3 | | Storage Class | 11 - Combustible Solids |
| | BOC-12-ADO-OH Usage And Synthesis |
| Description | Boc-12-Ado-OH can be used as a PROTAC linker in the synthesis of PROTACs. Boc-12-Ado-OH is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine. | | Uses | Boc-12-Ado-OH can be used as a PROTAC linker in the synthesis of PROTACs. Boc-12-Ado-OH is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine. | | reaction suitability | reaction type: Boc solid-phase peptide synthesis |
| | BOC-12-ADO-OH Preparation Products And Raw materials |
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