5836-66-8 Usage
Uses
Used in Chemical Synthesis:
2,3-Dibromopropylmethyl ether is used as a chemical intermediate for the synthesis of various organic compounds. Its unique structure allows it to be a key component in the creation of a wide range of chemical products.
Used in Solvent Applications:
2,3-Dibromopropylmethyl ether is also utilized as a solvent in certain chemical reactions. Its ability to dissolve other substances makes it a valuable asset in the chemical industry, facilitating various processes that require the use of solvents.
Used in Chemical Reactions:
2,3-Dibromopropylmethyl ether serves as a reagent in chemical reactions, contributing to the formation of new compounds or aiding in the transformation of existing ones. Its reactivity is an important factor in its application in this context.
Used in Industrial Processes:
While the specific industrial applications may vary, 2,3-Dibromopropylmethyl ether is used in various industries for its chemical properties. Its versatility in chemical processes makes it a valuable resource across different sectors.
Safety Considerations:
Check Digit Verification of cas no
The CAS Registry Mumber 5836-66-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5836-66:
(6*5)+(5*8)+(4*3)+(3*6)+(2*6)+(1*6)=118
118 % 10 = 8
So 5836-66-8 is a valid CAS Registry Number.
5836-66-8Relevant articles and documents
NaIO4-Mediated Selective Oxidative Halogenation of Alkenes and Aromatics Using Alkali Metal Halides
Dewkar, Gajanan K.,Narina, Srinivasarao V.,Sudalai, Arumugam
, p. 4501 - 4504 (2007/10/03)
(Equation presented) NaIO4 oxidizes alkali metal halides efficiently in aqueous medium to halogenate alkenes and aromatics and produce the corresponding halo derivatives in excellent regio and stereoselectivity. The system also demonstrates the asymmetric version of bromo hydroxylation using β-cyclodextrin complexes, resulting in moderate ee.
Functionalised organosulfur donor molecules: Synthesis of racemic hydroxymethyl-, alkoxymethyl- and dialkoxymethyl-bis(ethylenedithio)tetrathiafulvalenes
Saygili, Nezire,Brown, R.James,Day, Peter,Hoelzl, Robert,Kathirgamanathan, Poopathy,Mageean, Eileen R,Ozturk, Turan,Pilkington, Melanie,Qayyum, Mohammed M.B,Turner, Scott S,Vorwerg, Lars,Wallis, John D
, p. 5015 - 5026 (2007/10/03)
Short synthetic routes to racemic derivatives of bis(ethylenedithio)tetrathiafulvalene carrying one hydroxymethyl (HMET), alkoxymethyl or dialkoxymethyl side chain are reported along with cyclic voltammetry measurements and conversion of HMET to (2:1) radical cation salts.
