303153-22-2

Basic information

• Product Name: 2-biphenyl-4-ylmethyl-1,1-dioxo-2,3,6,7-tetrahydro-1H-1λ⁶-[1,2]thiazepine-7-carboxylic acid isopropyl ester
• CAS NO: 303153-22-2
• Molecular Weight: 399.511
• Mol File: 303153-22-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-biphenyl-4-ylmethyl-1,1-dioxo-2,3,6,7-tetrahydro-1H-1λ⁶-[1,2]thiazepine-7-carboxylic acid isopropyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-biphenyl-4-ylmethyl-1,1-dioxo-2,3,6,7-tetrahydro-1H-1λ⁶-[1,2]thiazepine-7-carboxylic acid isopropyl ester(303153-22-2)
• EPA Substance Registry System: 2-biphenyl-4-ylmethyl-1,1-dioxo-2,3,6,7-tetrahydro-1H-1λ⁶-[1,2]thiazepine-7-carboxylic acid isopropyl ester(303153-22-2)

Safety Data

• Hazardous Substances Data: 303153-22-2(Hazardous Substances Data)

Upstream product

• 303153-15-3 C₁₆H₂₇NO₆S 
• 303153-14-2 C₁₃H₂₃NO₆S 
• 303153-13-1 allylsulfamoyl-acetic acid isopropyl ester 
• 303153-12-0 isopropyl (chlorosulfonyl)acetate 
• 303153-16-4 2-allylsulfamoyl-pent-4-enoic acid isopropyl ester 
• 303153-17-5 1,1-dioxo-1,3,6,7-tetrahydro-1λ⁶-[1,2]thiazepine-2,7-dicarboxylic acid 2-tert-butyl ester 7-isopropyl ester 

Relevant articles and documents

Ring-closing metathesis to a divergent endocyclic sulfonamide template

The efficient synthesis of a novel endocyclic sulfonamide template via a ring-closing metathesis methodology is reported. A solid-supported variant of the Grubbs catalyst is shown to be effective and the suitability of the template for both combinatorial derivatization and potential incorporation into peptidomimetics is demonstrated. (C) 2000 Published by Elsevier Science Ltd.