1341236-03-0

Basic information

• Product Name: C₂₁H₁₈N₄O₆S
• Synonyms: C₂₁H₁₈N₄O₆S
• CAS NO: 1341236-03-0
• Molecular Weight: 454.463
• Mol File: 1341236-03-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₁H₁₈N₄O₆S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₁H₁₈N₄O₆S(1341236-03-0)
• EPA Substance Registry System: C₂₁H₁₈N₄O₆S(1341236-03-0)

Safety Data

• Hazardous Substances Data: 1341236-03-0(Hazardous Substances Data)

Upstream product

• 6915-90-8 2,4-dinitro-5-phenoxybenzenamine 
• 72830-09-2 2-Chloromethyl-3,4-dimethoxy-pyridine; hydrochloride 
• 367-81-7 2,4-dinitro-5-fluoroaniline 
• 327-92-4 1,5-difluoro-2,4-dinitrobenzene 
• 1341235-98-0 C₂₁H₁₈N₄O₅S 
• 1341235-93-5 C₁₃H₉N₃O₃S 
• 1341235-85-5 C₁₂H₁₁N₃O₃ 

Downstream Products

• 1341236-08-5 C₂₁H₂₀N₄O₄S 

Relevant articles and documents

A reverse method for diversity introduction of benzimidazole to synthesize H+/K+-ATP enzyme inhibitors

A series of 2-[(2-pyridylmethyl)sulfinyl]benzimidazole derivatives were synthesized via a solution phase synthetic route using a reversal method of diversity introduction. Using this synthetic strategy, we obtained two key intermediates (4-A and 4-B) simultaneously, which allows us to introduce diversity points onto the benzimidazole part of the final product under reliable reaction conditions to identify potent H+/K+-ATP enzyme inhibitors. Compound 14l (IC50 = 1.6 × 10-5 M) was comparable with H+/K+-ATP enzyme inhibitor in vitro.