832744-33-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 14 carbon (C) atoms, 8 hydrogen (H) atoms, 1 bromine (Br) atom, and 1 iodine (I) atom.
Explanation
The compound consists of a benzene ring (a six-membered ring with alternating single and double bonds) and a phenyl group (a benzene ring attached to another atom or group). The phenyl group is further substituted with an ethynyl group (a triple-bonded carbon chain) and a 4-iodophenyl group (a phenyl group with an iodine atom attached to the 4th carbon).
Explanation
The term "brominated" indicates that the compound has a bromine atom covalently bonded to the benzene ring. This bromine atom is located at the 1st position (1-Bromo) of the benzene ring.
Explanation
The compound is used in various fields, including the synthesis of other organic compounds, research in chemistry, and potential applications in the development of materials and pharmaceutical products.
Explanation
Due to its chemical nature, 1-bromo-4-[2-(4-iodophenyl)ethynyl]benzene may pose certain hazards when handled or used. It is crucial to follow appropriate safety measures and protocols, such as wearing personal protective equipment (PPE) and working in a well-ventilated area, to minimize the risk of exposure or accidents.
Explanation
Some organic compounds, including brominated aromatic compounds, can be sensitive to external factors like light, heat, or moisture, which may cause them to degrade or react. It is essential to store and handle the compound in a controlled environment to maintain its stability and prevent unwanted reactions.
Explanation
The compound is likely to be soluble in organic solvents, such as dichloromethane, acetone, or ethanol, due to its nonpolar nature. This property is useful for its applications in organic synthesis and research.
Explanation
The melting point of a compound is the temperature at which it transitions from a solid to a liquid state. The exact melting point for 1-bromo-4-[2-(4-iodophenyl)ethynyl]benzene may vary, but it can be determined through experimental methods.
Explanation
The boiling point of a compound is the temperature at which it transitions from a liquid to a gas state. The exact boiling point for 1-bromo-4-[2-(4-iodophenyl)ethynyl]benzene may vary, but it can be determined through experimental methods.
Explanation
Density is the mass per unit volume of a substance. The density of 1-bromo-4-[2-(4-iodophenyl)ethynyl]benzene may vary, but it can be determined through experimental methods. Density can be an important factor in determining the compound's suitability for specific applications.
Structure
Aromatic compound with a benzene ring and a phenyl group substituted with an ethynyl and iodophenyl group
Brominated
Presence of a bromine atom
Applications
Organic synthesis, research purposes, materials science, and pharmaceuticals
Hazards
Potential hazards, proper safety measures and protocols required
Stability
May be sensitive to light, heat, or moisture
Solubility
Soluble in organic solvents
Melting Point
Varies depending on the specific compound
Boiling Point
Varies depending on the specific compound
Density
Varies depending on the specific compound
Check Digit Verification of cas no
The CAS Registry Mumber 832744-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,2,7,4 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 832744-33:
(8*8)+(7*3)+(6*2)+(5*7)+(4*4)+(3*4)+(2*3)+(1*3)=169
169 % 10 = 9
So 832744-33-9 is a valid CAS Registry Number.
832744-33-9Relevant articles and documents
4-iodophenyl substituted carborane derivative and preparation method thereof
-
Paragraph 0085; 0088, (2020/12/30)
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
Palladium-Catalyzed Desulfitative Cross-Coupling of Arylsulfonyl Hydrazides with Terminal Alkynes: A General Approach toward Functionalized Internal Alkynes
Qian, Liang-Wei,Sun, Mengli,Dong, Jianyu,Xu, Qing,Zhou, Yongbo,Yin, Shuang-Feng
supporting information, p. 6764 - 6769 (2017/07/15)
A palladium-catalyzed Sonogashira-type coupling between arylsulfonyl hydrazides and terminal alkynes via Ar(C)-S bond cleavage is disclosed, which enables the general synthesis of functionalized internal alkynes, especially the Br-substituted ones, in good to excellent yields under acid- and base-free conditions.
