28077-74-9

Basic information

• Product Name: 6-Iodo-2-hexyne
• Synonyms: 6-Iodo-2-hexyne
• CAS NO: 28077-74-9
• Molecular Formula: C₆H₉I
• Molecular Weight: 208.04
• Mol File: 28077-74-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-Iodo-2-hexyne(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Iodo-2-hexyne(28077-74-9)
• EPA Substance Registry System: 6-Iodo-2-hexyne(28077-74-9)

Safety Data

• Hazardous Substances Data: 28077-74-9(Hazardous Substances Data)

Upstream product

• 14267-92-6 1-chloro-4-pentyne 
• 74-88-4 methyl iodide 
• 68275-05-8 methanesulfonic acid hex-4-ynyl ester 
• 928-93-8 4-hexyn-1-ol 
• 85355-30-2 2-(R,S)-(hex-4-ynyloxy)tetrahydropyran 
• 62992-46-5 1-(tetrahydropyranyloxy)-4-pentyn 
• 5390-04-5 pent-1-yn-5-ol 
• 28077-73-8 6-chlorohex-2-yne 

Downstream Products

• 848312-48-1 (1E)-2-methyl-1-phenylnon-1-en-7-yn-3-ol 
• 1450851-73-6 (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-2-methyloct-6-ynoic acid 

Relevant articles and documents

STABILIZED POLYPEPTIDES AND USES THEREOF

The present invention provides inventive stabilized STAT polypeptides, pharmaceutical compositions thereof, and methods of making and using inventive stabilized STAT polypeptides.

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TRIAZOLE-CROSSLINKED AND THIOETHER-CROSSLINKED PEPTIDOMIMETIC MACROCYCLES

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The scope of catalytic enantioselective tandem carbonyl ylide formation - Intramolecular [3 + 2] cycloadditions

Catalytic enantioselective tandem carbonyl ylide formation-intramolecular 1,3-dipolar cycloaddition reactions of 2-diazo-3,6-diketoesters show promising scope in terms of asymmetric induction as the tethered alkene/alkyne dipolarophile component is varied. Cycloadditions were found to occur in moderate to very good yields, with a difference in ee exhibited by the electronically different 2-diazo-3,6-diketoesters 1, 25 and 33, 34. Values for ee of up to 90% for alkene dipolarophiles and up to 86% for alkyne dipolarophiles were obtained.

An investigation of l,4,7-tri(4-alkynyl)-l,4,7-triazacyclononanes: Ligand synthesis and metal co-ordination chemistry

Three triazacyclononanes bearing pendant alkynyl groups [l,4,7-tri(4-pentynyl)-l,4,7-triazacyclononane (ptacn), 1,4,7-tri(5-phenyl-4-pentynyl)-l,4,7-triazacyclononane (pptacn) and 1,4,7-tri(4-hexynyl)-1,4,7-triazacyclononane (4htacn)] have been synthesize

Synthesis of Arylcycloalkanes from ω-Alkenyl Benzylselenides

Arylcycloalkanes are produced from ω-alkenyl benzylselenides on reaction with alkyllithiums or on Lewis acid mediated electrophilic cyclisation.