471925-05-0

Basic information

• Product Name: Benzoic acid, 4-[[(phenylsulfonyl)amino]methyl]-, methyl ester
• CAS NO: 471925-05-0
• Molecular Formula: C15H15NO4S
• Molecular Weight: 305.354
• Mol File: 471925-05-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-[[(phenylsulfonyl)amino]methyl]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-[[(phenylsulfonyl)amino]methyl]-, methyl ester(471925-05-0)
• EPA Substance Registry System: Benzoic acid, 4-[[(phenylsulfonyl)amino]methyl]-, methyl ester(471925-05-0)

Safety Data

• Hazardous Substances Data: 471925-05-0(Hazardous Substances Data)

Upstream product

• 18469-52-8 methyl 4-(aminomethyl)benzoate 
• 98-09-9 benzenesulfonyl chloride 
• 6232-11-7 methyl 4-(aminomethyl)benzoate hydrochloride 

Downstream Products

• 720-75-2 methyl 4-phenylbenzoate 
• 591217-95-7 4-(benzenesulfonylamino-methyl)-N-benzyloxy-benzamide 
• 178693-27-1 4-(phenylsulfonamidomethyl)benzoic acid 

Relevant articles and documents

METHOD FOR THE METAL-FREE PREPARATION OF A BIARYL BY A PHOTOSPLICING REACTION AND THEIR USES

The present invention relates to a method for the metal-free preparation of a biaryl compound by a photosplicing reaction and its use in the preparation of chemical compounds, preferably of active ingredients e.g. in the fields of pharmaceuticals and agrochemicals. In particular, it refers to a method for the regiocontrolled preparation of a biaryl compound of formula (I): Ar-Ar' by photochemically reacting a precursor compound of formula (II): Ar-L-Ar' to form a biaryl compound of general formula: Ar-L-Ar' (II) → Ar-Ar' (I) wherein Ar and Ar', independently of each other, represent an unsubstituted or substituted C6-C20 aryl group or a heteroaryl group with 5–20 ring atoms selected from carbon, nitrogen, oxygen and sulfur, and L represents a group –X–Y–Z– as defined herein. The biaryl compounds are generally suitable as intermediates or key building blocks in a very broad spectrum of organic chemical syntheses and their respective utilities. Their use within the field of synthesis of active ingredients is an aspect of the invention, and their use in the preparation of pharmaceutically active ingredients is particularly preferred.

ABCA1 ELEVATING COMPOUNDS

The present invention provides compounds having the structure of Formula (I), wherein R1 is optionally substituted lower alkyl, optionally substituted cycloaikyl, or optionally substituted aryl; R2 is hydrogen, carboxyalkyl, optional

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