(6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-ol - Names and Identifiers
Name | (S)-2-Nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-ol
|
Synonyms | (6S)-2-nitro-5H,6H,7H-imidazo[2,1-b][1,3]oxazin-6-ol (S)-2-Nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-ol (S)-2-NITRO-6,7-DIHYDRO-5H-IMIDAZO[2,1-B][1,3]OXAZIN-6-OL (6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-ol (6S)-2-Nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-ol 5H-imidazo[2,1-b][1,3]oxazin-6-ol, 6,7-dihydro-2-nitro-, (6S)- 5H-Imidazo[2,1-b][1,3]oxazin-6-ol, 6,7-dihydro-2-nitro-, (6S)-
|
CAS | 187235-08-1
|
InChI | InChI=1/C6H7N3O4/c10-4-1-8-2-5(9(11)12)7-6(8)13-3-4/h2,4,10H,1,3H2/t4-/m0/s1 |
(6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-ol - Physico-chemical Properties
Molecular Formula | C6H7N3O4
|
Molar Mass | 185.14 |
Density | 1.91±0.1 g/cm3(Predicted) |
Boling Point | 446.2±55.0 °C(Predicted) |
Flash Point | 223.662°C |
Solubility | Chloroform, DCM, Methanol |
Vapor Presure | 0mmHg at 25°C |
Appearance | Solid |
Color | White |
pKa | 13.21±0.20(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | 1.765 |
(6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-ol - Introduction
(S)-2-nitro-6, 7-dihydro-5H-imidazo [2,1-b][1,3] oxazin-6-ol is an organic compound, have the following properties, uses, methods and safety information:
Nature:
-Appearance: A white crystal or crystalline powder
-Molecular formula: C9H7N3O3
-Molecular weight: 209.17g/mol
-Melting Point: 156-159 ° C
-Insoluble in water, soluble in organic solvents such as methylene chloride
-Has a slight odor and fumigation
-Combustible, release toxic gas when burning
Use:
- (S)-2-nitro-6, 7-dihydro-5h-imidazo [2,1-b][1,3] Oxazin-6-ol is an important intermediate compound, which has a wide range of applications in the field of drug synthesis.
-It is mainly used for the synthesis of anticancer drugs, antiviral drugs and other biologically active molecules.
Method:
- (S)-2-nitro-6, 7-dihydro-5h-imidazo [2,1-b][1,3] The preparation of oxazin-6-ol usually uses chemical synthesis methods and requires multiple reactions.
-The specific preparation method may vary depending on the researcher and the research conditions, but usually includes the synthesis of imidazole derivatives, cyclization reaction and nitration reaction steps.
Safety Information:
-This compound has potential risks to humans and the environment and is a toxic substance.
-Wear appropriate personal protective equipment such as gloves, goggles and lab coats during operation.
-Avoid contact with skin, eyes and respiratory tract, and ingestion or inhalation of substances. If exposed to the substance, immediately flush the affected area with plenty of water and seek medical attention.
-During storage, it should be stored in a closed, cool, dry place, and stored separately from other chemicals.
-When disposing of waste, follow local environmental regulations to ensure safe disposal.
Last Update:2024-04-09 02:00:43