193882-72-3

Basic information

• Product Name: Benzoic acid, 5-iodo-2-(1-methylethoxy)-, methyl ester
• CAS NO: 193882-72-3
• Molecular Formula: C11H13IO3
• Molecular Weight: 320.127
• Mol File: 193882-72-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 5-iodo-2-(1-methylethoxy)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 5-iodo-2-(1-methylethoxy)-, methyl ester(193882-72-3)
• EPA Substance Registry System: Benzoic acid, 5-iodo-2-(1-methylethoxy)-, methyl ester(193882-72-3)

Safety Data

• Hazardous Substances Data: 193882-72-3(Hazardous Substances Data)

Upstream product

• 75-30-9 2-iodo-propane 
• 4068-75-1 methyl 5-iodosalicylate 
• 75-26-3 isopropyl bromide 

Downstream Products

• 1147012-18-7 methyl 5-[2-(methylsulfanyl)phenoxy]-2-(propan-2-yloxy)benzoate 
• 1033264-70-8 2-Isopropoxy-5-(2-methoxy-phenylethynyl)-benzoic acid 
• 1117834-39-5 2-Isopropoxy-5-phenylethynyl-benzoic acid methyl ester 
• 1033264-67-3 2-isopropoxy-5-trimethylsilanylethynyl-benzoic acid methyl ester 
• 1063677-03-1 2-Isopropoxy-5-(2-methoxy-phenylethynyl)-benzoic acid methyl ester 
• 193882-71-2 5-iodo-2-isopropoxy-benzoic acid 

Relevant articles and documents

Alkylacetylene substituted Acyltryptophanols

The present invention relates to acyltryptophanols of the general formula I, in which R1, R2, R3, Q and X have the meaning as defined in the description. The compounds according to the invention are effective FSH antagonists and can be used for example fo

Alpha-alkyl substituted N-acyltryptophanols

The present invention relates to α-alkyl substituted N-acyltryptophanols of the formula I in which R1, R2, R3, R4, R5, R6, Q, X and W have the meaning as defined in the description. The compounds according to the invention are effective FSH antagonists and can be used for example for fertility control in men or in women, or for the prevention and/or treatment of osteoporosis.

Discovery of potent and orally active 3-alkoxy-5-phenoxy-N-thiazolyl benzamides as novel allosteric glucokinase activators

Identification and synthesis of novel 3-alkoxy-5-phenoxy-N-thiazolyl benzamides as glucokinase activators are described. Removal of an aniline structure of the prototype lead (2a) and incorporation of an alkoxy or phenoxy substituent led to the identifica