37942-55-5

Basic information

• Product Name: (1S)-1-(2,3-dimethoxy-6-nitrophenyl)ethanol
• Synonyms: 1-(4,5-dimethoxy-2-nitrophenyl)ethanol;Benzenemethanol, 4,5-dimethoxy-α-methyl-2-nitro-
• CAS NO: 37942-55-5
• Molecular Formula: C₁₀H₁₃NO₅
• Molecular Weight: 227.2139
• Mol File: 37942-55-5.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 394.8°C at 760 mmHg
• Flash Point: 192.6°C
• Density: 1.259g/cm³
• Vapor Pressure: 6.08E-07mmHg at 25°C
• Refractive Index: 1.547
• PKA: 13.66±0.20(Predicted)
• CAS DataBase Reference: (1S)-1-(2,3-dimethoxy-6-nitrophenyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S)-1-(2,3-dimethoxy-6-nitrophenyl)ethanol(37942-55-5)
• EPA Substance Registry System: (1S)-1-(2,3-dimethoxy-6-nitrophenyl)ethanol(37942-55-5)

Safety Data

• Hazardous Substances Data: 37942-55-5(Hazardous Substances Data)

Usage

Description

(1S)-1-(2,3-dimethoxy-6-nitrophenyl)ethanol is a chiral chemical compound with the molecular formula C10H13NO5. It features a nitro group and two methoxy groups attached to a phenyl ring, along with an ethanol functional group. The "S" in its name signifies its specific stereochemical configuration. (1S)-1-(2,3-dimethoxy-6-nitrophenyl)ethanol plays a significant role in organic synthesis and pharmaceutical research, where it is utilized as a reagent and intermediate. Its potential extends to the development of drugs and other biologically active molecules.

Uses

Used in Organic Synthesis:
(1S)-1-(2,3-dimethoxy-6-nitrophenyl)ethanol is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, facilitating the creation of complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, (1S)-1-(2,3-dimethoxy-6-nitrophenyl)ethanol serves as an intermediate. It is valuable for the development of new drugs and biologically active molecules due to its unique structural features and reactivity.
Used in Drug Development:
(1S)-1-(2,3-dimethoxy-6-nitrophenyl)ethanol is utilized in the development of drugs, potentially contributing to the creation of novel therapeutic agents that target specific biological pathways or conditions.
Used in the Synthesis of Biologically Active Molecules:
(1S)-1-(2,3-dimethoxy-6-nitrophenyl)ethanol is also employed in the synthesis of biologically active molecules, which may have applications in medicine, agriculture, and other fields where such molecules can exert specific biological effects.

Upstream product

• 4101-32-0 4',5'-dimethoxy-2'-nitroacetophenone 
• 917-54-4 methyllithium 
• 20357-25-9 6-nitroveratraldehyde 
• 1131-62-0 1-(3,4-dimethoxyphenyl)ethanone 
• 75-24-1 trimethylaluminum 
• 91-16-7 1,2-dimethoxybenzene 

Downstream Products

• 293765-23-8 p-<(α-methyl-6-nitroveratryloxycarbonyl)oxy>nitrobenzene 
• 144619-12-5 α-(4,5-dimethoxy-2-nitro)phenylethyl bromide 
• 268739-35-1 bis[1-(4,5-dimethoxy-2-nitrophenyl)ethyl]-N,N-diisopropylphosphoramidite 
• 250292-63-8 4-(4',5'-dimethoxy-α'-methyl-2'-nitrobenzyloxycarbonyloxy)-3,5-dimethylbenzaldehyde 
• 293765-18-1 2-methyl-acrylic acid 2-{2-[1-(4,5-dimethoxy-2-nitro-phenyl)-ethoxycarbonylamino]-ethoxy}-ethyl ester 
• 250292-61-6 4-(4',5'-dimethoxy-α'-methyl-2'-nitrobenzyloxy)-3,5-dimethylbenzaldehyde 
• 250292-72-9 4-(4',5'-dimethoxy-α'-methyl-2'-nitrobenzyloxy)-3,5-dimethylbenzyl fluoride 
• 250292-66-1 4-(4',5'-dimethoxy-α'-methyl-2'-nitrobenzyloxy)-3,5-dimethylbenzyl alcohol 
• 250292-74-1 4-(4',5'-dimethoxy-α'-methyl-2'-nitrobenzyloxy)-3,5-dimethylbenzyl bromide 
• 250292-73-0 4-(4',5'-dimethoxy-α'-methyl-2'-nitrobenzyloxy)-3,5-dimethylbenzyl chloride 
• 250292-80-9 4-(4',5'-dimethoxy-α'-methyl-2'-nitrobenzyloxycarbonyloxy)-3,5-dimethylbenzyl bromide 
• 250292-79-6 4-(4',5'-dimethoxy-α'-methyl-2'-nitrobenzyloxycarbonyloxy)-3,5-dimethylbenzyl chloride 
• 250292-78-5 4-(4',5'-dimethoxy-α'-methyl-2'-nitrobenzyloxycarbonyloxy)-3,5-dimethylbenzyl fluoride 
• 250292-68-3 4-(4',5'-dimethoxy-α'-methyl-2'-nitrobenzyloxycarbonyloxy)-3,5-dimethylbenzyl alcohol 

Relevant articles and documents

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Dehydroxyalkylative halogenation of C(aryl)-C bonds of aryl alcohols

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