876275-37-5

Basic information

• Product Name: Glycine, N-(carboxymethyl)-N-[4-(hydroxymethyl)-2-oxo-2H-1-benzopyran-7-yl]-
• CAS NO: 876275-37-5
• Molecular Formula: C14H13NO7
• Molecular Weight: 307.26
• Mol File: 876275-37-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Glycine, N-(carboxymethyl)-N-[4-(hydroxymethyl)-2-oxo-2H-1-benzopyran-7-yl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-(carboxymethyl)-N-[4-(hydroxymethyl)-2-oxo-2H-1-benzopyran-7-yl]-(876275-37-5)
• EPA Substance Registry System: Glycine, N-(carboxymethyl)-N-[4-(hydroxymethyl)-2-oxo-2H-1-benzopyran-7-yl]-(876275-37-5)

Safety Data

• Hazardous Substances Data: 876275-37-5(Hazardous Substances Data)

Upstream product

• 1009081-33-7 C₁₈H₂₀N₂O₈ 
• 1031721-25-1 O-{{7-[bis(carboxymethyl)amino]coumarin-4-yl}methyl} (S)-(4-acetamidophenyl) thiocarbonate 
• 1031721-24-0 (S)-{{7-[bis(carboxymethyl)amino]coumarin-4-yl}methyloxycarbonyl}-N-Fmoc-L-cysteine 
• 1031721-23-9 N-{{7-[bis(carboxymethyl)amino]coumarin-4-yl}methyloxycarbonyl}-L-norepinephrine 
• 1031721-22-8 {7-[bis(carboxymethyl)amino]coumarin-4-yl}methyl 2-phenylethyl carbonate 
• 1031721-21-7 (E)-{7-[bis(carboxymethyl)amino]coumarin-4-yl}methyl 2-methoxy-4-[(8-methylnon-6-enamido)methyl]phenyl carbonate 
• 1031721-20-6 {7-[bis(carboxymethyl)amino]coumarin-4-yl}methyl phenyl carbonate 
• 1031721-16-0 {7-[bis(carboxymethyl)amino]coumarin-4-yl}methyl phenylacetate 

Relevant articles and documents

Synthesis and photocleavage of 7-[{Bis(carboxymethyl)amino}-coumarin-4-yl] methyl-caged neurotransmitters

7-[{Bis(carboxymethyl)amino}coumarin-4-yl]methyl-caged neurotransmitters (glutamate and GABA) were synthesized. Both caged compounds showed sufficient stability in the dark, were water-soluble at pH 7.2 without using organic solvents, and exhibited relati

Coumarinylmethyl esters for ultrafast release of high concentrations of cyclic nucleotides upon one- and two-photon photolysis

(Chemical Equation Presented) Shedding light: Efficient activation of cyclic nucleoside monophosphates (cNMPs) can be achieved upon one- and two-photon flash photolysis of novel photolabile coumarinylmethyl esters of cAMP and cGMP (A = adenosine, G = guanosine) as well as their 8-bromosubstituted derivatives. The phototriggers show high solubility in water and permit space- and time-resolved investigations of the molecular mechanisms of cyclic nucleotide dependent processes.