630104-26-6

Basic information

• Product Name: 1-Triazene, 3,3-diethyl-1-(4-iodophenyl)-
• CAS NO: 630104-26-6
• Molecular Formula: C10H14IN3
• Molecular Weight: 303.146
• Mol File: 630104-26-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1-Triazene, 3,3-diethyl-1-(4-iodophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Triazene, 3,3-diethyl-1-(4-iodophenyl)-(630104-26-6)
• EPA Substance Registry System: 1-Triazene, 3,3-diethyl-1-(4-iodophenyl)-(630104-26-6)

Safety Data

• Hazardous Substances Data: 630104-26-6(Hazardous Substances Data)

Upstream product

• 53694-87-4 1-azido-4-iodo-benzene 
• 109-89-7 diethylamine 
• 540-37-4 p-aminoiodobenzene 

Downstream Products

• 468751-10-2 C₁₃H₁₇N₃O 
• 134856-57-8 1-[4-[2-(trimethylsilyl)ethynyl]phenyl]-3,3-diethyltriazene 
• 850836-42-9 C₃₄H₄₅N₃Si 
• 850195-88-9 [3-butyl-5-(4-iodo-phenylethynyl)-thiophen-2-ylethynyl]-trimethyl-silane 
• 850195-87-8 C₂₂H₂₅N₃S 
• 850195-84-5 C₂₅H₃₃N₃SSi 
• 850195-89-0 C₄₀H₃₉N₃S₂ 
• 850195-90-3 (3-butyl-5-{4-[3-butyl-5-(4-iodo-phenylethynyl)-thiophen-2-ylethynyl]-phenylethynyl}-thiophen-2-ylethynyl)-trimethyl-silane 
• 850195-85-6 C₄₃H₄₇N₃S₂Si 
• 155064-31-6 3,3-diethyl-1-(4-ethynylbenzene)-1-triazene 
• 874115-26-1 1-Bromo-2,5-bis-dodecyloxy-4-(4-iodo-phenylethynyl)-benzene 
• 874115-24-9 C₄₂H₆₆BrN₃O₂ 
• 874115-25-0 C₄₇H₇₅N₃O₂Si 
• 874115-29-4 C₇₈H₁₁₂BrIO₄ 

Relevant articles and documents

4-iodophenyl substituted carborane derivative and preparation method thereof

The invention discloses a 4-iodophenyl carborane derivative and a preparation method thereof. Commercialized organic reagents 4-iodoaniline and a diacetonitrile decaborate complex and several easily-synthesized substituted alkynes are adopted as the start

Synthesis of triazene-substituted homoconjugated push-pull chromophores by formal [2?+?2] cycloadditions

1-(4-Ethynylphenyl)-3,3-dialkyltriaz-1-enes, well-known building blocks for branched dendrimer syntheses, were utilized as a new type of electron-donor component in formal [2 + 2] cycloadditions. The click-type, atom-economic reactions proceed efficiently

Aromatic fluoro-de-triazenation with boron trifluoride diethyl etherate under non-protic acid conditions

Fluoro-de-triazenation of 3,3-diethyl-1-aryltriazenes can be achieved by conventional or under microwave heating in carbon tetrachloride, in the presence of boron trifluoride diethyl etherate without any protic acid to avoid corresponding unwanted byproduct formation.