cas 50591-22-5|| where to buy 1-Methyl-1H-benzimidazol-5-ol

Product Name:1-Methyl-1H-benzimidazol-5-ol

IUPAC Name:1-methyl-1H-1,3-benzodiazol-5-ol

Packing Unit	Available Stock	Price($)
CM154913-5g	in stock	ɐȦ
CM154913-10g	in stock	ƱȷȦ
CM154913-25g	in stock	Ǖǲɐ

For R&D use only.

Inquiry Form

Chemical Name

CAS Number

Quantity*

Required Specifications*
(Assay %, Material Grade etc.)

Contact Name*

Contact Email*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 50591-22-5 regularly via the above email.

Additional Notes

Verification code*

refresh

: CAS NO:50591-22-5; Molecular Formula:C8H8N2O; Melting Point:-; Smiles Code:OC1=CC=C2N(C)C=NC2=C1; Density:

: Catalog Number:CM154913; Molecular Weight:148.17; Boiling Point:337.7±34.0°C at 760 mmHg; MDL No:MFCD00456136; Storage:Store at 2-8°C.

: Benzimidazoles; Benzimidazole is a benzo derivative of imidazole. It is a kind of bicyclic aromatic organic compounds, which is formed by fusing a six-membered benzene ring and five-membered imidazole at positions 4 and 5 of imidazole ring. It is an important pharmacophore of many biologically active heterocyclic compounds with various pharmacological activities. Benzimidazoles and their derivatives have developed into dynamic heterocyclic systems due to their potency in a variety of biologically active compounds such as anticancer, bactericidal and antiviral drugs. Benzimidazoles are a class of therapeutic motifs with broad relevance in medicinal chemistry.

: Zongertinib; Boehringer’s zongertinib shows encouraging efficacy and tolerability profile in previously treated HER2 mutated lung cancer patients.
Zongertinib (also known as BI 1810631) is an investigational oral HER2-specific tyrosine kinase inhibitor (TKI) that is being developed as a potential treatment for HER2 mutated non-small cell lung cancer (NSCLC). Zongertinib was granted FDA Fast Track Designation in 2023, then in 2024 it was granted Breakthrough Therapy Designation by the U.S. FDA and China CDE for the treatment of adult patients with advanced NSCLC whose tumors have activating HER2 mutations, and who have received a prior systemic therapy.