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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Oxetane, 3-(bromomethyl)-3-methyl-

BrCC1(C)COC1 Request for Quotation
Chemical Name: Oxetane, 3-(bromomethyl)-3-methyl-
CAS Number: 78385-26-9
Product Number: AG005BEK(AGN-PC-0JMU6F)
Synonyms:
MDL No: MFCD02684290
Molecular Formula: C5H9BrO
Molecular Weight: 165.0284

Identification/Properties

Properties
BP:
162 °C at 760 mmHg
Storage:
2-8℃;
Form:
Liquid
Refractive Index:
1.4800 to 1.4840
Computed Properties
Molecular Weight:
165.03g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
163.984g/mol
Monoisotopic Mass:
163.984g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
68.5
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Bromomethyl)-3-methyloxetane is a versatile compound commonly used in chemical synthesis processes. Its unique structure and reactivity make it a valuable building block in the creation of various organic compounds. The bromine atom attached to the oxetane ring imparts specific properties that are beneficial for specific reactions and transformations in the laboratory.One significant application of 3-(Bromomethyl)-3-methyloxetane is in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and materials. Its bromomethyl group can undergo nucleophilic substitution reactions, allowing for the introduction of different functional groups or the modification of existing ones. This flexibility makes it a valuable intermediate in the production of diverse chemical compounds.Additionally, 3-(Bromomethyl)-3-methyloxetane can participate in ring-opening reactions, leading to the formation of various ring-expanded or ring-contracted compounds. These transformations are essential in the design and synthesis of molecular scaffolds with specific properties or functionalities. By leveraging the reactivity of this compound, chemists can access novel structures and generate libraries of compounds for further investigation in drug discovery and materials science.Overall, the strategic incorporation of 3-(Bromomethyl)-3-methyloxetane in chemical synthesis enables the efficient and controlled construction of complex organic molecules with tailored properties and functionalities. Its role as a key intermediate highlights its significance in driving innovation and exploration in the field of organic chemistry.