Acetylides
3-Ethynylanisole 97.0+%, TCI America™
CAS: 768-70-7 Molecular Formula: C9H8O Molecular Weight (g/mol): 132.16 MDL Number: MFCD00160810 InChI Key: ZASXCTCNZKFDTP-UHFFFAOYSA-N Synonym: 3-ethynylanisole,3-methoxyphenylacetylene,1-ethynyl-3-methoxy-benzene,benzene, 1-ethynyl-3-methoxy,3-ethynyl-1-methoxybenzene,1-etynyl-3-methoxy-benzene,3-ethynyl-anisole,m-methoxyphenylacetylene,3-ethynylanisole 96 PubChem CID: 640753 IUPAC Name: 1-ethynyl-3-methoxybenzene SMILES: COC1=CC=CC(=C1)C#C
2-Ethynylpyridine 97.0+%, TCI America™
CAS: 1945-84-2 Molecular Formula: C7H5N Molecular Weight (g/mol): 103.124 MDL Number: MFCD00041598 InChI Key: NHUBNHMFXQNNMV-UHFFFAOYSA-N Synonym: 2-ethynyl pyridine,2-pyridylacetylene,pyridine, 2-ethynyl,2-ethynyl-pyridine,pyridine, ethynyl,pyridin-2-yl acetylene,ethynylpyridine,ethynyl pyridine,ortho-ethynylpyridine PubChem CID: 137268 IUPAC Name: 2-ethynylpyridine SMILES: C#CC1=CC=CC=N1
Propargyltrimethylsilane, 80-90%, stabilized
CAS: 13361-64-3 Molecular Formula: C6H12Si Molecular Weight (g/mol): 112.25 MDL Number: MFCD00042922 InChI Key: ULYLMHUHFUQKOE-UHFFFAOYSA-N Synonym: propargyltrimethylsilane,silane, trimethyl-2-propynyl,trimethyl 2-propynyl silane,trimethyl prop-2-ynyl silane,trimethyl propargyl silane,silane, trimethyl-2-propyn-1-yl,trimethyl prop-2-yn-1-yl silane,trimethyl-2-propynylsilane,propargyl trimethylsilane,2-propynyltrimethylsilane PubChem CID: 83378 IUPAC Name: trimethyl(prop-2-ynyl)silane SMILES: C[Si](C)(C)CC#C
1-Hexadecyne, tech. 90%
CAS: 629-74-3 Molecular Formula: C16H30 Molecular Weight (g/mol): 222.42 MDL Number: MFCD00015084 InChI Key: UCIDYSLOTJMRAM-UHFFFAOYSA-N Synonym: 1-hexadecyne,tetradecylacetylene,acmc-209nbc PubChem CID: 12396 IUPAC Name: hexadec-1-yne SMILES: CCCCCCCCCCCCCCC#C
Phenyl propargyl ether, 98+%
CAS: 13610-02-1 Molecular Formula: C9H8O Molecular Weight (g/mol): 132.16 MDL Number: MFCD00048107 InChI Key: AIQRJSXKXVZCJO-UHFFFAOYSA-N Synonym: phenyl propargyl ether,prop-2-ynyloxy benzene,prop-2-yn-1-yloxy benzene,phenyl 2-propynyl ether,benzene, 2-propynyloxy,3-phenoxy-1-propyne,2-propynyloxy benzene,phenylpropargyl ether,prop-2-ynyloxybenzene,ether, phenyl 2-propynyl PubChem CID: 83613 IUPAC Name: prop-2-ynoxybenzene SMILES: C#CCOC1=CC=CC=C1
Phenyl propargyl ether, 97%
CAS: 13610-02-1 Molecular Formula: C9H8O Molecular Weight (g/mol): 132.16 MDL Number: MFCD00048107 InChI Key: AIQRJSXKXVZCJO-UHFFFAOYSA-N Synonym: phenyl propargyl ether,prop-2-ynyloxy benzene,prop-2-yn-1-yloxy benzene,phenyl 2-propynyl ether,benzene, 2-propynyloxy,3-phenoxy-1-propyne,2-propynyloxy benzene,phenylpropargyl ether,prop-2-ynyloxybenzene,ether, phenyl 2-propynyl PubChem CID: 83613 IUPAC Name: prop-2-ynoxybenzene SMILES: C#CCOC1=CC=CC=C1
1-Tetradecyne, tech. 90%
CAS: 765-10-6 Molecular Formula: C14H26 Molecular Weight (g/mol): 194.362 MDL Number: MFCD00015076 InChI Key: DZEFNRWGWQDGTR-UHFFFAOYSA-N Synonym: 1-tetradecyne,tetradecyne,tetradec-1-in,acmc-1bfxn PubChem CID: 69823 IUPAC Name: tetradec-1-yne SMILES: CCCCCCCCCCCCC#C
Medchemexpress LLC Tert-butyl (5-hydroxypentyl)carbamate | 75178-90-4 | MFCD01862955 | ≥95.0% | 203.28 g/mol | C10H21NO3 | 5 G
Tert-butyl (5-hydroxypentyl)carbamate is a Boc-protected amino alcohol used as a synthetic building block and linker in organic and medicinal chemistry. The molecule combines an acid-labile Boc-protected amine with a terminal hydroxyl, allowing selective deprotection and subsequent functionalization for conjugation or further synthesis.
- Boc-protected amine removable under mild acidic conditions.
- Terminal hydroxyl enables esterification, etherification, or activation for coupling.
- Useful as a bifunctional building block for organic and medicinal chemistry.
- Molecular weight 203.28 g/mol; formula C10H21NO3.
Medchemexpress LLC 5-(Boc-amino)-1-pentanol | 75178-90-4 | MFCD01862955 | ≥97.0% | 203.28 g/mol | C10H21NO3 | 25 G
5-(Boc-amino)-1-pentanol is a Boc-protected amino alcohol used as a versatile linker and intermediate in organic synthesis and medicinal chemistry. It features a tert-butoxycarbonyl (Boc) protected amine and a primary hydroxyl group that permit orthogonal functionalization - the hydroxyl can be derivatized or replaced, and the Boc group can be removed under mild acidic conditions to reveal the free amine.
- Contains a Boc-protected amine and a primary hydroxyl.
- Enables orthogonal functionalization for multi-step syntheses.
- Hydroxyl group suitable for derivatization or conjugation reactions.
- Boc group deprotects under mild acidic conditions to yield free amine.
- High purity (≥97%) appropriate for research applications.
- Solid material stable at room temperature with defined solvent storage conditions.
Medchemexpress LLC 5-(Boc-amino)-1-pentanol | 75178-90-4 | MFCD01862955 | ≥97.0% | 203.28 g/mol | C10H21NO3 | 10 G
5-(Boc-amino)-1-pentanol is a Boc-protected amino alcohol used as a versatile linker and building block in organic and medicinal chemistry. The tert-butoxycarbonyl (Boc) group protects the amine during multi-step syntheses, while the primary hydroxyl group enables subsequent functionalization and conjugation.
- Boc-protected amine for orthogonal protection strategies.
- Primary hydroxyl enables esterification and coupling reactions.
- High purity suitable for synthesis (≥97%).
- Available in multiple small-scale packages for research use.
- Compact molecular weight facilitates incorporation into small molecules.
Medchemexpress LLC Tert-butyl N-(5-hydroxypentyl)carbamate | 75178-90-4 | MFCD01862955 | >97.0% | 203.28 g·mol⁻1 | C10H21NO3 | 1 G
5-(Boc-amino)-1-pentanol is a Boc-protected 5-aminopentanol used as a versatile intermediate and linker in organic and medicinal chemistry. It contains a tert-butoxycarbonyl protected amine and a primary alcohol, enabling selective deprotection and further functionalization for synthesis of peptides, small molecules, and conjugates.
- Boc-protected amine enables selective deprotection workflows.
- Primary alcohol allows further derivatization and coupling reactions.
- High purity suitable for synthetic and medicinal chemistry applications.
- Defined storage stability in solvent and bulk formats.
- Useful as a linker for conjugation and building-block synthesis.