1. Home
  2. Benzene, 1-bromo-4-heptyl-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

Benzene, 1-bromo-4-heptyl-

CCCCCCCc1ccc(cc1)Br Request for Quotation
Chemical Name: Benzene, 1-bromo-4-heptyl-
CAS Number: 76287-49-5
Product Number: AG003B19(AGN-PC-0KKWML)
Synonyms:
MDL No:
Molecular Formula: C13H19Br
Molecular Weight: 255.1940

Identification/Properties

Properties
BP:
296.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
1.5170-1.5190
Computed Properties
Molecular Weight:
255.199g/mol
XLogP3:
5.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
6
Exact Mass:
254.067g/mol
Monoisotopic Mass:
254.067g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
125
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H227-H315-H319-H335
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


1-Bromo-4-heptylbenzene, a versatile chemical compound, serves as a valuable reagent in chemical synthesis processes. With its unique structure and properties, it finds significant application in organic chemistry for constructing complex molecules and creating various functional materials. As a brominated alkylbenzene derivative, 1-Bromo-4-heptylbenzene offers a reactive bromine atom that acts as a key intermediate in diverse synthetic pathways, facilitating the formation of new carbon-carbon and carbon-heteroatom bonds through substitution, elimination, or coupling reactions. This compound acts as a crucial building block for the creation of pharmaceuticals, agrochemicals, and other fine chemicals, enabling the synthesis of intricate organic compounds with tailored properties and functionalities. In addition, 1-Bromo-4-heptylbenzene plays a vital role in material science applications, contributing to the development of advanced polymers, liquid crystals, and other specialty materials through controlled polymerization and functionalization processes. Its versatility and reactivity make it a valuable tool for chemists and researchers seeking to explore new synthetic routes and design novel molecules with specific characteristics and applications.