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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)-

1-(bromomethyl)-4-methylcyclohexane

BrCC1CCC(CC1)C Request for Quotation
Chemical Name: 1-(bromomethyl)-4-methylcyclohexane
CAS Number: 21857-32-9
Product Number: AG00I48O(AGN-PC-00MNPS)
Synonyms:
MDL No: MFCD16657517
Molecular Formula: C8H15Br
Molecular Weight: 191.1087

Identification/Properties

Computed Properties
Molecular Weight:
191.112g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
190.036g/mol
Monoisotopic Mass:
190.036g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
72.6
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(Bromomethyl)-4-methylcyclohexane, also known as BMCMH, is a versatile organic compound widely used in chemical synthesis. With its unique structure, BMCMH serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. In organic synthesis, BMCMH is commonly employed as a reactive intermediate in the formation of complex molecular structures through substitution and addition reactions. Its bromomethyl group enables selective functionalization of cyclohexane derivatives, making it a valuable tool for synthetic chemists seeking to introduce specific functional groups with high regioselectivity. In addition, BMCMH's cyclohexyl backbone provides a stable and rigid scaffold for further modifications, enhancing the overall efficiency and control of multi-step synthesis processes. By harnessing the reactivity and structural features of 1-(Bromomethyl)-4-methylcyclohexane, chemists can access a wide range of novel compounds with tailored properties and applications in diverse fields of chemistry.