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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-Thiophenecarboxylic acid, 2-amino-4-ethyl-5-methyl-, ethyl ester

CCOC(=O)c1c(N)sc(c1CC)C Request for Quotation
Chemical Name: 3-Thiophenecarboxylic acid, 2-amino-4-ethyl-5-methyl-, ethyl ester
CAS Number: 82546-91-6
Product Number: AG004UGK(AGN-PC-0JUR43)
Synonyms:
MDL No:
Molecular Formula: C10H15NO2S
Molecular Weight: 213.2966

Identification/Properties

Computed Properties
Molecular Weight:
213.295g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
213.082g/mol
Monoisotopic Mass:
213.082g/mol
Topological Polar Surface Area:
80.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
210
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate is a versatile compound widely utilized in chemical synthesis. Its unique structure and properties make it a valuable building block for the production of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, Ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate serves as a key intermediate in the preparation of heterocyclic compounds. Its presence in a synthesis pathway can introduce essential functional groups, such as amino, carboxylate, and ethyl moieties, which can significantly impact the final product's properties and reactivity.This compound is particularly valuable in the synthesis of pharmaceutical compounds due to its ability to impart desirable biological activities. By incorporating Ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate into a molecule, chemists can fine-tune the compound's pharmacokinetic profile, enhance its potency, or even improve its solubility.Additionally, Ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate finds applications in the development of agrochemicals, where its structural motifs can contribute to the herbicidal, fungicidal, or insecticidal properties of the final product. Its versatility in chemical synthesis makes it a valuable tool for creating functional molecules across various industries.