64287-98-5

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The chemical structure describes the arrangement of atoms in the molecule and the type of bonding between them.

Explanation

A diol is a compound with two hydroxyl (OH) groups, and a derivative of cyclohexane is a compound derived from cyclohexane by modifying its structure.

Explanation

The presence of bromine atoms in the molecule contributes to its reactivity and properties.

Explanation

The compound's chemical structure and properties make it suitable for various applications across different industries.

Explanation

Due to potential hazards and risks to health and the environment, it is essential to handle and use this chemical compound carefully and follow safety guidelines.

Explanation

The compound may pose risks to human health and the environment if not handled and used properly, making it crucial to follow safety protocols.

Chemical structure

Cyclohexane with two hydroxyl (OH) groups at the 1 and 2 positions and two bromine (Br) atoms at the 4 and 5 positions.

Type of compound

Diol derivative of cyclohexane

Bromine content

Contains two bromine atoms

Applications

Organic synthesis, reagent in chemical reactions, pharmaceutical, agricultural, and manufacturing industries.

Safety precautions

Handle with caution, follow proper safety protocols

Potential hazards

Risks to health and the environment

Upstream product

• 1165952-92-0 cyclohexa-1,4-diene 
• 62199-53-5 4,5-dibromocyclohexene 
• 42846-36-6 trans-4,5-dibromo-1-cyclohexene 

Downstream Products

• 80409-80-9 (2α,3aβ,5β,6α,7aβ)-5,6-dibromohexahydro-2-phenyl-1,3-benzodioxole 
• 104286-31-9 C₁₉H₁₈O₂ 
• 104286-32-0 C₁₉H₁₈O₂ 
• 80409-74-1 (2α,3aα,7aα)-3a,7a-dihydro-2-phenyl-1,3-benzodioxole 
• 80409-79-6 C₂₇H₂₂O₂ 
• 80409-76-3 C₂₇H₂₂O₂ 
• 104286-28-4 2-Methoxy-3a,7a-dihydro-benzo[1,3]dioxole 
• 104286-31-9 C₁₉H₁₈O₂ 
• 104286-32-0 C₁₉H₁₈O₂ 
• 1039105-48-0 10,11-bis(phenylsulfonyl)-4,4-dimethyl-3,5-dioxa-tricyclo[5.2.2.0(2.6)]undec-8-ene 
• 51622-32-3 rac-3,4-Dibrom-adipinsaeure 
• 102698-38-4 (R)-1-(7,8-Dimethoxy-2-oxa-3-aza-bicyclo[2.2.2]oct-5-en-3-yl)-3,3,3-trifluoro-2-methoxy-2-phenyl-propan-1-one 
• 102698-40-8 (4R,5R,6R)-4-Amino-5,6-dimethoxy-cyclohex-2-enol 
• 102698-33-9 racem. trans-5,6-Dimethoxy-1,3-cyclohexadien 

Relevant academic research and scientific papers

Base-Mediated Fragmentation of Bicyclic Dihydro-3,6-oxazines: Transformation of Nitroso Diels-Alder Cycloadducts

Nitroso Diels-Alder cycloadditions of benzene oxide with various acyl-nitroso derivatives are described. Treatment of these cycloadducts with methyllithium results in a fast fragmentation reaction, leading to highly functionalized cyclic amino alcohols. T

Compound and method of producing organic semiconductor device

A method of producing an organic semiconductor device is provided in which a layer composed of an organic semiconductor having excellent crystallinity and orientation in a low-temperature region can be formed, and the device can be produced in the air. The method includes forming a layer composed of an organic semiconductor precursor on a base body and irradiating the organic semiconductor precursor with light, wherein the organic semiconductor precursor is a porphyrin compound or an azaporphyrin compound having in its molecule at least one of the structure represented by the following general formula (1) or (2):

NOVEL COMPOUND AND METHOD OF PRODUCING ORGANIC SEMICONDUCTOR DEVICE

A method of producing an organic semiconductor device is provided in which a layer composed of an organic semiconductor having excellent crystallinity and orientation in a low-temperature region can be formed, and the device can be produced in the air. The method includes forming a layer composed of an organic semiconductor precursor on a base body and irradiating the organic semiconductor precursor with light, wherein the organic semiconductor precursor is a porphyrin compound or an azaporphyrin compound having in its molecule at least one of the structure represented by the following general formula (1) or (2):

An efficient and highly stereoselective synthesis of gala-Quercitol from 1,4-cyclohexadiene

gala-Quercitol was synthesized from 1,4-cyclohexadiene in seven steps and overall yield of 68%. Reaction of 5,6-dibromo-2,2-dimethylhexahydro-1,3-benzodioxole, synthesized from 1,4-cyclohexadiene in three steps, with excess NaOMe gave (3aα,5α,7aα)-5-metho