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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)-

Octane, 1-bromo-3,7-dimethyl-

BrCCC(CCCC(C)C)C Request for Quotation
Chemical Name: Octane, 1-bromo-3,7-dimethyl-
CAS Number: 3383-83-3
Product Number: AG003E3Y(AGN-PC-0JMPRY)
Synonyms:
MDL No:
Molecular Formula: C10H21Br
Molecular Weight: 221.1777

Identification/Properties

Properties
BP:
225.7 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Refractive Index:
n20/D 1.455(lit.)
Computed Properties
Molecular Weight:
221.182g/mol
XLogP3:
5.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
6
Exact Mass:
220.083g/mol
Monoisotopic Mass:
220.083g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
78.9
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Bromo-3,7-dimethyloctane is a versatile compound often utilized in chemical synthesis as a valuable building block for various organic reactions. With its unique structure containing a bromine atom and multiple methyl groups, this compound demonstrates significant reactivity and selectivity in a wide range of transformations.In organic synthesis, 1-Bromo-3,7-dimethyloctane serves as an important alkylating agent, allowing the introduction of the 1-bromo-3,7-dimethyloctyl group into target molecules. This group can act as a functional handle for further modifications, enabling the synthesis of more complex organic compounds. The bromine atom provides a reactive site for nucleophilic substitution reactions, leading to the formation of new carbon-carbon or carbon-heteroatom bonds.Furthermore, the presence of multiple methyl groups in 1-Bromo-3,7-dimethyloctane imparts steric effects that can influence the regioselectivity and stereochemistry of chemical reactions. By carefully manipulating the positioning of these methyl groups, chemists can control the outcome of reactions and steer the synthesis towards specific products with desired properties.Overall, 1-Bromo-3,7-dimethyloctane plays a crucial role in enabling the construction of complex organic molecules with tailored structures and functionalities, making it an indispensable tool in the toolbox of synthetic chemists.