Ethyl 2-amino-5-ethylthiophene-3-carboxylate, 98%

Name: Ethyl 2-amino-5-ethylthiophene-3-carboxylate, 98% | 4507-13-5
Brand: J&K Chemical
SKU: JK795396_1_G
Price: 62.0 USD
Availability: InStock

Cat. No JK795396_1_G

Vendor: J&K Chemical

Product Information

Product Name

Ethyl 2-amino-5-ethylthiophene-3-carboxylate, 98%

Brand Name

J&K

Product Number

795396

CAS

4507-13-5

Molecular Formula

C9H13NO2S

Molecular Weight

199.27

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

78263

IUPAC Name

ethyl 2-amino-5-ethylthiophene-3-carboxylate

InChI Key

WJZCEFNVWQJNQI-UHFFFAOYSA-N

SMILES

CCC1=CC(=C(S1)N)C(=O)OCC

Properties

Melting Point

73-74

Safety Information

Signal Word

Warning

Hazard Statement

H316

H320

H335

Precautionary Statement

P261

P271

P319

P405

P501

P332+P317

P264+P265

P305+P351+P338

P337+P317

P304+P340

P403+P233

References Data Source From Pubchem

Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells

Publication Name: Biochemical and Biophysical Research Communications

Publication Date: 2023-10-30

DOI: 10.1016/j.bbrc.2023.08.050

A quantitative high-throughput screen identifies compounds that lower expression of the SCA2-and ALS-associated gene ATXN2

Publication Name: The Journal of biological chemistry

Publication Date: 2022-08

DOI: 10.1016/j.jbc.2022.102228

Structure-Guided Discovery of Selective Mcl-1 Inhibitors

Publication Name: Synfacts

Publication Date: 2019-09-17

DOI: 10.1055/s-0039-1690939

A new method for the synthesis of esters of β-thiophenecarboxylic acids

Publication Name: Chemistry of Heterocyclic Compounds

Publication Date: 1967-11

DOI: 10.1007/bf00474869

Synthesis of derivatives of 2-aminothiophene and of thienoxazine

Publication Name: Chemistry of Heterocyclic Compounds

Publication Date: 1967-07

DOI: 10.1007/bf00509426

Ethyl 2-amino-5-ethylthiophene-3-carboxylate, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells

A quantitative high-throughput screen identifies compounds that lower expression of the SCA2-and ALS-associated gene ATXN2

Structure-Guided Discovery of Selective Mcl-1 Inhibitors

A new method for the synthesis of esters of β-thiophenecarboxylic acids

Synthesis of derivatives of 2-aminothiophene and of thienoxazine