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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-Thiophenecarboxaldehyde, 5-chloro-

Clc1ccc(s1)C=O Request for Quotation
Chemical Name: 2-Thiophenecarboxaldehyde, 5-chloro-
CAS Number: 7283-96-7
Product Number: AG00349C(AGN-PC-0JLTF6)
Synonyms:
MDL No:
Molecular Formula: C5H3ClOS
Molecular Weight: 146.5947

Identification/Properties

Properties
BP:
221.1°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Stability:
Air Sensitive
Refractive Index:
n20/D 1.604(lit.)
Computed Properties
Molecular Weight:
146.588g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
145.959g/mol
Monoisotopic Mass:
145.959g/mol
Topological Polar Surface Area:
45.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
96.4
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:
H302+H312+H332
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Chlorothiophene-2-carbaldehyde is a versatile chemical used in various chemical synthesis processes. One of its key applications is as a building block in the synthesis of complex organic molecules. This compound can serve as a key intermediate in the production of pharmaceuticals, agrochemicals, and materials with specific properties.Its unique structure, combining a chlorothiophene ring with a carbaldehyde functional group, allows for diverse chemical reactions and transformations. In organic synthesis, 5-Chlorothiophene-2-carbaldehyde can be employed in multi-step sequences to introduce specific functionalities or structural motifs into target molecules. Additionally, this compound can participate in cross-coupling reactions, heterocyclic chemistry, and other transformations to access a wide range of chemical structures.The versatility of 5-Chlorothiophene-2-carbaldehyde makes it a valuable tool for chemists working in drug discovery, materials science, and other fields that require the precise manipulation of molecular structures. By leveraging its reactivity and compatibility with various synthetic methods, researchers can access new compounds with potential applications in medicine, agriculture, and industry.