2-Acetamido-4-(chloromethyl)-1,3-thiazole, 95%

Name: 2-Acetamido-4-(chloromethyl)-1,3-thiazole, 95% | 7460-59-5
Brand: J&K Chemical
SKU: JK816461_250_MG
Price: 29.6 USD
Availability: OutOfStock

Cat. No JK816461_250_MG

Vendor: J&K Chemical

Product Information

Product Name

2-Acetamido-4-(chloromethyl)-1,3-thiazole, 95%

Brand Name

J&K

Product Number

816461

CAS

7460-59-5

Molecular Formula

C6H7ClN2OS

Molecular Weight

190.65

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

81963

IUPAC Name

N-4-(chloromethyl)-1,3-thiazol-2-ylacetamide

InChI Key

NBUKMHXINQOFDI-UHFFFAOYSA-N

SMILES

CC(=O)NC1=NC(=CS1)CCl

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

Cysteine S-conjugate β-lyases: important roles in the metabolism of naturally occurring sulfur and selenium-containing compounds, xenobiotics and anticancer agents

Publication Name: Amino Acids

Publication Date: 2010-03-22

DOI: 10.1007/s00726-010-0552-0

Role of Cysteine S-Conjugate β-Lyases in the Bioactivation of Renal Toxicants

Publication Name: Advances in Bioactivation Research

Publication Date: 2008

DOI: 10.1007/978-0-387-77300-1_12

From α-Halo Ketones and Aminothiocarbonyl Compounds

Publication Name: Science of Synthesis

Publication Date: 2002

2-Acetamido-4-(chloromethyl)-1,3-thiazole, 95%

Product Information

General 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

Cysteine S-conjugate β-lyases: important roles in the metabolism of naturally occurring sulfur and selenium-containing compounds, xenobiotics and anticancer agents

Role of Cysteine S-Conjugate β-Lyases in the Bioactivation of Renal Toxicants

From α-Halo Ketones and Aminothiocarbonyl Compounds