77759-08-1

Basic information

• Product Name: 2-(2,6-dinitrophenyl)ethanol
• Synonyms: 2-(2,6-dinitrophenyl)ethanol;Benzeneethanol, 2,6-dinitro-;2,6-dinitroBenzeneethanol
• CAS NO: 77759-08-1
• Molecular Formula: C₈H₈N₂O₅
• Molecular Weight: 212.15952
• Mol File: 77759-08-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 69 °C
• Boiling Point: 348.0±27.0 °C(Predicted)
• Appearance: /
• Density: 1.479±0.06 g/cm3(Predicted)
• PKA: 14.40±0.10(Predicted)
• CAS DataBase Reference: 2-(2,6-dinitrophenyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,6-dinitrophenyl)ethanol(77759-08-1)
• EPA Substance Registry System: 2-(2,6-dinitrophenyl)ethanol(77759-08-1)

Safety Data

• Hazardous Substances Data: 77759-08-1(Hazardous Substances Data)

Usage

General Description

2-(2,6-dinitrophenyl)ethanol, also known as DNPE, is a chemical compound with the molecular formula C8H7N3O6. It is a yellow powder that is used primarily as an intermediate in the synthesis of pharmaceuticals and dyes. DNPE is also used in the production of antioxidants and stabilizers for plastics and rubber. It is considered to be a hazardous chemical and should be handled with care due to its toxicity and potential for explosive decomposition when heated. Additionally, it is classified as a skin and eye irritant, and prolonged or repeated exposure may cause skin sensitization.

Upstream product

• 50-00-0 formaldehyd 
• 606-20-2 2,6-dinitrotoluene 
• 602-01-7 1-methyl-2,3-dinitrobenzene 

Downstream Products

• 52536-99-9 1-(2-chloroethyl)-2,6-dinitrobenzene 
• 118742-89-5 2-(2,6-diaminophenyl)ethanol 
• 179691-22-6 2-(2,6-dinitrophenyl)ethyl chloroformate 
• 115444-93-4 methanesulfonic acid 2-(2,6-dinitro-phenyl)-ethyl ester 
• 195992-08-6 2,6-dinitrostyrene 
• 179691-37-3 5'-O-(2-(2,6-dinitrophenyl)ethoxycarbonyl)thymidine 
• 2380-94-1 1H-indol-4-ol 
• 85926-99-4 4-hydroxyindoline 
• 4769-97-5 4-nitro-1H-indoIe 
• 84807-26-1 4-nitro-2,3-dihydro-1H-indole 

Relevant articles and documents

4,5,6 and 7-indole and indoline derivatitives, their preparation and use

A substituted 4-, 5-, 6-, and 7-indole derivative of Formula (I) wherein A is a group having formula (IIA), (IIB), (IIC) wherein X, U, Y, R3to R12, Z, W, n and m are as defined above. The compounds are potent serotonin reuptake inhib

Nucleoside derivatives with photolabile protective groups

The invention relates to nucleoside derivatives having photolabile protective groups of the general formula (I) STR1 in which R1 =H, NO2, CN, OCH3, halogen or alkyl or alkoxyalkyl having 1 to 4 C atoms R2 =H, OCH3 R3 =H, F, Cl, Br, NO2 R4 =H, halogen, OCH3, or an alkyl radical having 1 to 4 C atoms R5 =H or a usual functional group for preparing oligonucleotides R6 =H, OH, halogen or XR8, where X=O or S and R8 represents a protective group usual in nucleotide chemistry, B=adenine, cytosine, guanine, thymine, uracil, 2,6-diaminopurin-9-yl, hypoxanthin-9-yl, 5-methylcytosin-1-yl, 5-amino-4-imidazolcarboxamid-1-yl, or 5-amino-4-imidazolcarboxamid-3-yl, where in the case of B=adenine, cytosine or guanine, the primary amino function optionally exhibits a permanent protective group. These derivatives may be used for the light-controlled synthesis of oligonucleotides on a DNA chip.

A facile synthesis of 4-hydroxy- and 4-aminoindoles through corresponding indolines

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