37482-16-9

Basic information

• Product Name: etheno-AMP
• Synonyms: etheno-AMP
• CAS NO: 37482-16-9
• Molecular Formula: C12H14N5O7P
• Molecular Weight: 371.242621
• Mol File: 37482-16-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 2.21g/cm³
• Refractive Index: 1.913
• CAS DataBase Reference: etheno-AMP(CAS DataBase Reference)
• NIST Chemistry Reference: etheno-AMP(37482-16-9)
• EPA Substance Registry System: etheno-AMP(37482-16-9)

Safety Data

• Hazardous Substances Data: 37482-16-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H14N5O7P/c18-8-6(3-23-25(20,21)22)24-12(9(8)19)17-5-14-7-10-13-1-2-16(10)4-15-11(7)17/h1-2,4-6,8-9,12,18-19H,3H2,(H2,20,21,22)/t6-,8-,9-,12-/m1/s1

Upstream product

• 107-20-0 2-chloroethanal 
• 61-19-8 5'-adenosine monophosphate 
• 56860-78-7 bromoacetaldehyde hydrate 

Relevant articles and documents

Synthesis of 2-azido-1,N6-etheno and 2-azido analogs of deoxyadenosine as nucleotide photoaffinity probes

We prepared 2-azido-1,N6-etheno-2'-deoxyadenosine 5'-monophosphate (7b) by activation of the 2-thio analog 4b by two methods. In the preferred method, 4b was treated with 2,4-dinitrofluorobenzene in 50% aqueous acetonitrile, and the resultant thioether was cleaved with hydrazoic acid, yielding the 2-azido-1,N6-etheno analog 7b in 70% isolated yield. N-bromoacetamide oxidized the etheno group of 7b, giving the 2-azido analog of dAMP 9b in 78% yield.

Modification of adenine and cytosine derivatives with bromoacetaldehyde

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