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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)-

3-Bromo-4-chloro isopropyl benzene

CC(c1ccc(c(c1)Br)Cl)C Request for Quotation
Chemical Name: 3-Bromo-4-chloro isopropyl benzene
CAS Number: 90350-25-7
Product Number: AG019FYS(AGN-PC-0WALE4)
Synonyms:
MDL No:
Molecular Formula: C9H10BrCl
Molecular Weight: 233.5327

Identification/Properties

Computed Properties
Molecular Weight:
233.533g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
231.965g/mol
Monoisotopic Mass:
231.965g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
11
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-1-chloro-4-isopropylbenzene is a versatile chemical compound that finds significant application in chemical synthesis. Due to its unique properties, this compound is commonly used as a building block in the production of various organic compounds. Its precise chemical structure allows for selective reactions, making it a valuable tool in synthetic chemistry.Chemists utilize 2-Bromo-1-chloro-4-isopropylbenzene as a key intermediate in the synthesis of complex organic molecules. Its halogen substituents provide strategic functional groups that can undergo a variety of reactions, such as nucleophilic substitutions and cross-coupling reactions. This compound's reactivity and stability make it a valuable precursor in the creation of pharmaceuticals, agrochemicals, and specialty chemicals.In addition to its role as a synthetic intermediate, 2-Bromo-1-chloro-4-isopropylbenzene serves as a valuable tool in the study of reaction mechanisms and organic synthesis strategies. Chemists can leverage its unique structure to explore new synthetic pathways and develop innovative strategies for molecule construction. Its versatility and compatibility with a wide range of reaction conditions make it a valuable asset in the pursuit of novel chemical transformations and compound synthesis.