64283-87-0

Basic information

• Product Name: (4-iodobutyl)Benzene
• Synonyms: (4-iodobutyl)Benzene
• CAS NO: 64283-87-0
• Molecular Formula: C₁₀H₁₃I
• Molecular Weight: 260.11469
• Mol File: 64283-87-0.mol
• Article Data: 35

Chemical Properties

• Boiling Point: 148-151 °C(Press: 15 Torr)
• Appearance: /
• Density: 1.494±0.06 g/cm3(Predicted)
• CAS DataBase Reference: (4-iodobutyl)Benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (4-iodobutyl)Benzene(64283-87-0)
• EPA Substance Registry System: (4-iodobutyl)Benzene(64283-87-0)

Safety Data

• Hazardous Substances Data: 64283-87-0(Hazardous Substances Data)

Usage

Description

(4-iodobutyl)Benzene, also known as 1-iodo-4-(phenylmethyl)butane, is a chemical compound belonging to the class of iodobenzenes. It features a molecular formula of C10H13I, a molecular weight of 258.12 g/mol, and a boiling point of 285-286 degrees Celsius. This colorless liquid interacts with iodobenzene, iodine compound, and benzenes, and is valued for its unique chemical properties.

Uses

Used in Organic Synthesis:
(4-iodobutyl)Benzene is used as a reagent in organic synthesis for its unique chemical properties, facilitating various chemical reactions and contributing to the formation of different compounds.
Used in Pharmaceutical Industry:
(4-iodobutyl)Benzene is used as a precursor for the development of biologically active compounds, potentially leading to the creation of new pharmaceutical products.
Used in Agrochemical Industry:
(4-iodobutyl)Benzene is also utilized in the agrochemical industry, where it may be involved in the synthesis of compounds with applications in agriculture, such as pesticides or fertilizers.

Upstream product

• 65512-08-5 4-phenylbutyl methanesulfonate 
• 2046-17-5 methyl 3-(benzyl)propanoate 
• 54555-84-9 benzyl iodoethyl ether 
• 1462-37-9 bromoethyl-2-benzyl ether 
• 13633-25-5 1-Bromo-4-phenylbutane 
• 2270-20-4 5-Phenylpentanoic acid 
• 104-51-8 1-butylbenzene 
• 1229444-44-3 N-methyl-N-[4-(diphenylphosphino)benzyl]pyrrolidinium bromide 
• 3360-41-6 4-phenyl-butan-1-ol 
• 1229444-43-2 4-(diphenylphosphino)-benzyltrimethylammonium bromide 
• 124-63-0 methanesulfonyl chloride 
• 1821-12-1 4-Phenylbutyric acid 
• 3277-89-2 phenethylmagnesium bromide 
• 112775-09-4 4-phenylbutyl 4-methylbenzenesulfonate 

Downstream Products

• 119-64-2 tetralin 
• 768-56-9 4-Phenylbut-1-ene 
• 104-51-8 1-butylbenzene 
• 1560-06-1 1-phenyl-2-butene 
• 1026251-92-2 6-Methyl-3-(4-phenyl-butoxy)-pyridine-2-carbaldehyde 
• 1252645-09-2 C₃₅H₅₄O₂Si 
• 1286739-95-4 2-(1,1-difluoro-5-phenylpentylsulfonyl)pyridine 
• 1316742-26-3 2-(RS)-(2-aminobenzoylamino)-6-phenylhexanoic acid ethyl ester 
• 1316742-36-5 2-(RS)-{2-[(1H-indole-2-carbonyl)amino]benzoylamino}-6-phenylhexanoic acid ethyl ester 
• 1316741-79-3 2-(RS)-{2-[(1H-indole-2-carbonyl)amino]benzoylamino}-6-phenylhexanoic acid 
• 1316742-08-1 2-(RS)-amino-6-phenylhexanoic acid hydrochloride 
• 1316742-15-0 2-(RS)-amino-6-phenylhexanoic acid ethyl ester hydrochloride 
• 80887-21-4 2-acetylamino-2-(4-phenyl-butyl)malonic acid diethyl ester 
• 102472-04-8 4-phenylbutyl 5-phenylpentanoate 

Relevant articles and documents

Nucleophilic substitution reactions of unbranched alkyl amines using triazine reagents

Since amines are present in many organic, biological, and drug molecules, a strategy of synthesizing desired compounds by nucleophilic substitution reactions of these amines is very attractive. By using triazine reagents, we have found that nucleophilic substitution reactions of unbranched alkyl amines via morpholine derivatives are feasible. This method can be performed under milder reaction conditions than those in previously reported methods.

Visible-Light-Induced Nickel-Catalyzed Cross-Coupling with Alkylzirconocenes from Unactivated Alkenes

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Substrate and Catalyst Effects in the Enantioselective Copper-Catalysed C–H Insertion Reactions of α-Diazo-β-oxo Sulfones

Excellent enantioselectivities of up to 98 % ee are achieved by employing the copper-bis(oxazoline)-NaBARF catalyst system in the C–H insertion reactions of α-diazo-β-oxo sulfones. The influence of variation of the bis(oxazoline) ligand, copper salt, additive and substrate on both the efficiency and the enantioselectivities of these intramolecular C–H insertion reactions has been explored. Optimum enantioselectivities are achieved with phenyl and diphenyl ligands across the substrate series.