1. Home
  2. [2,2'-Bithiophene]-5-carboxylic acid, 4-amino-, methyl ester

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

[2,2'-Bithiophene]-5-carboxylic acid, 4-amino-, methyl ester

COC(=O)c1sc(cc1N)c1cccs1 Request for Quotation
Chemical Name: [2,2'-Bithiophene]-5-carboxylic acid, 4-amino-, methyl ester
CAS Number: 169759-79-9
Product Number: AG00AOPD(AGN-PC-0KK82Y)
Synonyms:
MDL No:
Molecular Formula: C10H9NO2S2
Molecular Weight: 239.3140

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Methyl 4-amino-[2,2'-bithiophene]-5-carboxylate is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various organic molecules due to its unique chemical properties. Its application in synthetic organic chemistry involves reactions with a variety of other compounds to produce complex structures with specific functionalities.In particular, Methyl 4-amino-[2,2'-bithiophene]-5-carboxylate is used in the synthesis of pharmaceuticals, agrochemicals, and materials with specialized properties. It can undergo various chemical transformations such as acylation, alkylation, and condensation reactions to form new carbon-carbon or carbon-heteroatom bonds.Furthermore, its aromatic structure containing a bithiophene core provides opportunities for the development of novel materials for applications in organic electronics, optoelectronics, and sensors. This compound's versatility and synthetic utility make it a valuable asset in the toolkit of synthetic chemists for the construction of diverse organic compounds with tailored properties and functions.