3814-32-2 Usage
Uses
Used in Organic Synthesis:
Cycloheptane, (bromomethyl)is used as a starting material in organic synthesis for the production of various chemicals and pharmaceuticals. Its bromomethyl group allows for a range of reactions, making it a valuable intermediate in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Cycloheptane, (bromomethyl)is employed as a building block for the development of new drugs. Its unique structure can be modified to create novel compounds with potential therapeutic applications.
Used in Pesticide Manufacturing:
Cycloheptane, (bromomethyl)is used in the manufacturing of pesticides. Its chemical properties make it suitable for the production of active ingredients in various agrochemicals, contributing to crop protection and yield enhancement.
Used in Dye Production:
In the dye industry, Cycloheptane, (bromomethyl)is utilized for the synthesis of dyes. Its reactivity and structural features enable the creation of a wide range of dyes with different color properties and applications.
Used as a Solvent in Chemical Reactions:
Cycloheptane, (bromomethyl)can be used as a solvent for chemical reactions. Its ability to dissolve a variety of substances makes it a useful component in various chemical processes, facilitating reactions and improving yields.
Used as a Reagent in Organic Chemistry:
In organic chemistry, Cycloheptane, (bromomethyl)serves as a reagent for various reactions. Its bromomethyl group can participate in a range of organic transformations, making it a valuable tool for chemists in their research and development efforts.
Safety Precautions:
It is important to handle Cycloheptane, (bromomethyl)with caution due to its flammable nature and potential harmful effects if inhaled or ingested. Proper safety measures, such as wearing protective gear and working in well-ventilated areas, should be taken to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 3814-32-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,1 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3814-32:
(6*3)+(5*8)+(4*1)+(3*4)+(2*3)+(1*2)=82
82 % 10 = 2
So 3814-32-2 is a valid CAS Registry Number.
3814-32-2Relevant academic research and scientific papers
Hindson, Andrew C.,Walton, John C.
, p. 3237 - 3241 (1990)
The EPR spectra of cycloheptylmethyl, cyclohept-4-enylmethyl and 1,3-dioxacyclohept-5-enylmethyl radicals have been observed.The cycloheptylmethyl radical spectrum shows only a single, average conformation, but for the cycloheptene and dioxacycloheptene rings the CH2* group proved to be a useful probe of the conformations.The preferred conformation of the 1,3-dioxacycloheptene ring was found to depend on the type of substitution at C(2).For the 2-CH2* radical, twist-boat and chair conformers were observed with an Arrhenius activation barrier to inversion of 5 kcal mol-1.For the 2-CH3, 2-CH2* radical the main conformation was the twist-boat.For the 2-Ph, 2CH2* radical the main conformation was the chair; the rotation of the CH2* group was found to be restricted by a barrier of ca. 7.5 kcal mol-1, probably because of steric interaction from two syn axial hydrogens on C(4) and C(7).
Heterocyclic compounds as inhibitors of rotomase enzymes
-
, (2008/06/13)
Compounds of the formula: wherein R1, Y, W, A and R2are as defined above are inhibitors of rotamase enzymes in particular FKBP-12 and FKBP-52. The compounds therefore moderate neuronal regeneration and outgrowth and can be used for treating neurological disorders arising from neurodegenerative diseases and nerve damage.
