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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)-

Thiophenecarboxylic acid, ethyl ester

CCOC(=O)c1cccs1 Request for Quotation
Chemical Name: Thiophenecarboxylic acid, ethyl ester
CAS Number: 2810-04-0
Product Number: AG003Q5F(AGN-PC-0CBISD)
Synonyms:
MDL No:
Molecular Formula: C7H8O2S
Molecular Weight: 156.2022

Identification/Properties

Properties
BP:
218.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Stability:
Air Sensitive
Refractive Index:
n20/D 1.526(lit.)
Computed Properties
Molecular Weight:
156.199g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
156.025g/mol
Monoisotopic Mass:
156.025g/mol
Topological Polar Surface Area:
54.5A^2
Heavy Atom Count:
10
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:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 2-thiophenecarboxylate is a versatile chemical compound commonly used in chemical synthesis for its ability to introduce the thiophene moiety into various organic molecules. As a key building block in the synthesis of pharmaceuticals, agrochemicals, and materials, this compound plays a crucial role in the creation of new and innovative products. With its unique structure and reactivity, Ethyl 2-thiophenecarboxylate enables chemists to access a diverse array of functionalized thiophene derivatives, offering opportunities for the development of novel therapeutic agents, pesticide formulations, and advanced materials. By incorporating Ethyl 2-thiophenecarboxylate into their synthetic routes, researchers can harness its synthetic potential to explore new chemical space and drive innovation in the field of organic chemistry.