99584-95-9

Basic information

• Product Name: 1,2-DIBROMO-3,3-DIMETHYL-1-BUTENE
• Synonyms: 1,2-DIBROMO-3,3-DIMETHYL-1-BUTENE
• CAS NO: 99584-95-9
• Molecular Formula: C6H10Br2
• Molecular Weight: 241.95
• Mol File: 99584-95-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 188.322°C at 760 mmHg
• Flash Point: 64.238°C
• Appearance: /
• Density: 1.65
• Vapor Pressure: 0.832mmHg at 25°C
• Refractive Index: 1.5120-1.5170
• Storage Temp.: Refrigerator
• CAS DataBase Reference: 1,2-DIBROMO-3,3-DIMETHYL-1-BUTENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DIBROMO-3,3-DIMETHYL-1-BUTENE(99584-95-9)
• EPA Substance Registry System: 1,2-DIBROMO-3,3-DIMETHYL-1-BUTENE(99584-95-9)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 99584-95-9(Hazardous Substances Data)

Usage

General Description

1,2-Dibromo-3,3-dimethyl-1-butene is a chemical compound with the molecular formula C6H10Br2. It is a colorless liquid that is commonly used as an intermediate in the synthesis of other organic compounds. 1,2-DIBROMO-3,3-DIMETHYL-1-BUTENE is known for its use in the production of pharmaceuticals, agrochemicals, and fine chemicals. It is a highly reactive compound due to the presence of the bromine atoms, and it is important to handle it with caution. Additionally, it is also used as a building block in the production of polymers and other organic materials. Overall, 1,2-Dibromo-3,3-dimethyl-1-butene is a versatile and important chemical compound in various industrial processes.

InChI:InChI=1/C6H10Br2/c1-6(2,3)5(8)4-7/h4H,1-3H3

Upstream product

• 13601-86-0 1-bromo-3,3-dimethyl-1-butyne 
• 917-92-0 3,3-Dimethylbut-1-yne 
• 7726-95-6 bromine 
• 64-19-7 acetic acid 

Downstream Products

• 131079-29-3 2-(2,2-dimethylethyl)butenedinitrile 

Relevant articles and documents

Preparation method of dicyano compound

The invention relates to a preparation method of a dicyano compound, and particularly discloses a preparation method of a dicyano compound shown in a general formula (I), which is characterized in that the reaction formula is as follows: in the formula, R is selected from one of alkane, aromatic hydrocarbon or halogenated aromatic hydrocarbon; the acyl chloride compound as shown in the general formula (II) reacts with metal cyanide to generate an acyl cyanide compound as shown in a general formula (III), and after solvent extraction, the acyl cyanide compound directly reacts with diethyl cyanomethylphosphonate under a strong alkaline condition to generate the dicyano compound as shown in the general formula (I). By adopting the method disclosed by the invention, the process raw material cost is low, the by-product cuprous chloride is insoluble in the used solvent and is easy to recover, the used solvent in the process can be recovered and reused, and the method disclosed by the invention can simultaneously realize the technical effects of reducing the cost and reducing the environmental protection pressure.

Benzo-fused low symmetry metal-free tetraazaporphyrin and phthalocyanine analogs: Synthesis, spectroscopy, electro chemistry, and density functional theory calculations

A whole series of low-symmetry, metal-free tetrapyrrole analogs 1-11 ranging from tetraazaporphyrin H2TAP(tBu)4 to napthalocyanine H2Nc(tBu)4 via H2Pc(tBu) 4 have been designed and prepared. Their electronic structures have been spectroscopically and electrochemically investigated. Through the preparation of a series of tetrapyrrole compounds with just the same number of four tert-butyl substituents at similar positions of the macrocyclic ring, the effect intrinsic to the enlargement of the ring system has been easily extracted and understood. Along with the increase in the size of central conjugated system, the half-wave potentials of the first oxidation for 1-11 are shifted significantly to the negative direction. This is also true for the half-wave potentials of the first reduction process of this series of tetrapyrrole derivatives but in a slight manner. These results indicate that along with the ring extension, the energy of the HOMO increases significantly while that of the LUMO only slightly increases. The effect of the ring size of these tetrapyrrole compounds on the electronic absorption and fluorescence spectra is also clear: both the Q band and fluorescence shifts to longer wavelength with the increase in the number of fused benzene rings but with a diminishing increase due to the extending of the central conjugated system. These results were reasonably explained by considering the energy levels of frontier molecular orbitals of the series of compounds obtained by the calculations using DFT method at the B3LYP/6-31G(d) level.