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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)-

4-chlorothiophene-2-carbonitrile

Clc1cc(sc1)C#N Request for Quotation
Chemical Name: 4-chlorothiophene-2-carbonitrile
CAS Number: 910553-55-8
Product Number: AG006F0P(AGN-PC-03Y02T)
Synonyms:
MDL No:
Molecular Formula: C5H2ClNS
Molecular Weight: 143.5941

Identification/Properties

Properties
BP:
210.8±20.0°C at 760 mmHg
Storage:
Light sensitive;Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
143.588g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
142.96g/mol
Monoisotopic Mass:
142.96g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
128
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chlorothiophene-2-carbonitrile is a versatile compound widely used in chemical synthesis processes due to its distinctive properties and reactivity. This compound serves as a valuable building block in the preparation of various organic molecules and pharmaceutical intermediates. Its unique structure containing a chlorine atom and a cyano group attached to a thiophene ring allows for selective functionalization and enables the creation of complex molecular structures.In chemical synthesis, 4-Chlorothiophene-2-carbonitrile can be employed as a key intermediate in the production of agrochemicals, pharmaceuticals, and specialty chemicals. Its reactivity enables the introduction of additional functional groups through various chemical transformations such as nucleophilic substitution, Suzuki coupling, and halogenation reactions. By utilizing 4-Chlorothiophene-2-carbonitrile as a starting material, chemists can access a diverse array of compounds with tailored properties and functions.Furthermore, the presence of a cyano group in 4-Chlorothiophene-2-carbonitrile offers synthetic chemists the opportunity to modify the compound through traditional cyanation reactions, facilitating the synthesis of new molecules with enhanced biological activities or physical properties. Overall, the strategic incorporation of 4-Chlorothiophene-2-carbonitrile in chemical synthesis processes enables the efficient construction of complex organic molecules with importance in various industrial sectors.