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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)-

2-Thiophenemethanol, 5-bromo-

OCc1ccc(s1)Br Request for Quotation
Chemical Name: 2-Thiophenemethanol, 5-bromo-
CAS Number: 79387-71-6
Product Number: AG005216(AGN-PC-009231)
Synonyms:
MDL No:
Molecular Formula: C5H5BrOS
Molecular Weight: 193.0616

Identification/Properties

Properties
BP:
267.104°C at 760 mmHg
Storage:
Keep in dry area;-10 ℃;
Form:
Liquid
Refractive Index:
1.6010 to 1.6050
Computed Properties
Molecular Weight:
193.058g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
191.924g/mol
Monoisotopic Mass:
191.924g/mol
Topological Polar Surface Area:
48.5A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
78.8
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


The versatile compound 5-Bromothien-2-yl)methanol plays a crucial role in modern chemical synthesis methods. As a key building block, it is commonly utilized in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. This compound serves as a valuable starting material for the creation of various heterocyclic compounds due to its reactive bromine group and the unique thienyl ring structure. In organic synthesis, (5-Bromothien-2-yl)methanol acts as a strategic intermediate in the production of complex molecules, enabling chemists to efficiently introduce functional groups and modify molecular properties. Its significance extends to the development of novel drugs, crop protection agents, and specialized materials with tailored properties, making it an indispensable tool for researchers and industry professionals alike.