24558-92-7

Basic information

• Product Name: ADENOSINE 5'-MONOPHOSPHO-MORPHOLIDATE 4-MORPHOLINE-N,N'-DICYCLOHEXYLCARBOXAMIDINE SALT
• Synonyms: ADENOSINE 5'-MONOPHOSPHO-MORPHOLIDATE 4-MORPHOLINE-N,N'-DICYCLOHEXYLCARBOXAMIDINE SALT;ADENOSINE 5'-MONOPHOSPHOMORPHOLIDATE;adenosine 5'-monophosphomorpholidate, MDCC salt
• CAS NO: 24558-92-7
• Molecular Formula: C₁₄H₂₁N₆O₇P*C₁₇H₃₁N₃O
• Molecular Weight: 709.77
• Product Categories: Biochemicals and Reagents;Nucleosides, Nucleotides, Oligonucleotides;Nucleotide Analogs
• Mol File: 24558-92-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: −20°C
• Solubility: Methanol
• CAS DataBase Reference: ADENOSINE 5'-MONOPHOSPHO-MORPHOLIDATE 4-MORPHOLINE-N,N'-DICYCLOHEXYLCARBOXAMIDINE SALT(CAS DataBase Reference)
• NIST Chemistry Reference: ADENOSINE 5'-MONOPHOSPHO-MORPHOLIDATE 4-MORPHOLINE-N,N'-DICYCLOHEXYLCARBOXAMIDINE SALT(24558-92-7)
• EPA Substance Registry System: ADENOSINE 5'-MONOPHOSPHO-MORPHOLIDATE 4-MORPHOLINE-N,N'-DICYCLOHEXYLCARBOXAMIDINE SALT(24558-92-7)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38-40
• Safety Statements: 24-36-45
• WGK Germany: 3
• Hazardous Substances Data: 24558-92-7(Hazardous Substances Data)

Usage

Uses

Adenosine 5''-Monophosphomorpholidate 4-Morpholine-N,N''-dicyclohexylcarboxamidine salt is an intermediate in the synthesis of Flavine Adenine Dinucleotide.

Upstream product

• 110-91-8 morpholine 
• 61-19-8 5'-adenosine monophosphate 
• 538-75-0 dicyclohexyl-carbodiimide 

Downstream Products

• 53-84-9 NAD 
• 112345-60-5 1-((1R,2S,3R,4R)-4-((((((((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)hydroxyphosphoryl)oxy)oxidophosphoryl)oxy)methyl)-2,3-dihydroxycyclopentyl)-3-carbamoylpyridin-1-ium 
• 61-19-8 5'-adenosine monophosphate 
• 83285-83-0 Tiazofurin adenine dinucleotide 

Relevant articles and documents

Simple synthesis of P1P2-diadenosine 5′-pyrophosphate

Pyrophosphate-linked coenzymes play essential roles in several biochemical systems. Symmetrical diadenosine-5′-pyrophosphate (Ap2A) has been synthesized from adenosine-5′-phosphate in virtually quantitative yield. The simple procedure is carried out in an