4-Phenylmorpholine
What is 4-Phenylmorpholine, cas no:92-53-5,a producer telling you the result.
CAS NO.92-53-5
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To begin with, let us tell you what is the basic information of 4-Phenylmorpholine ?
Molecular Formula |
C10H13NO |
Molecular Weight |
163.216 |
Density |
1.1±0.1 g/cm3 |
Boiling Point |
264.8±0.0 °C at 760 mmHg |
Flash Point |
80.6±27.7 °C |
Melting Point |
51-54 °C(lit.) |
Like many stuff, it has many synonyms as follows
EINECS 202-164-0 |
4-PHENYL MORPHOLINE |
Phenyl morpholine |
Morpholinobenzene |
MFCD00006166 |
4-Phenyl-morpholine |
Morpholine, 4-phenyl- |
MORPHOLINE,4-PHENYL |
N-phenyl-morpholine |
4-Phenylmorpholine |
First, the chemical is very special, some technical indexes as below
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toxicology data
The oral LD50 of rats is 930mg/kg.
Ecological data
Currently unavailable
Molecular structure data
1. Molar refractive index: 48.06
2. Molar volume (cm3/mol): 152.7
3. Waiting for Zhang Bi Rong (90.2K): 381.0
4. Surface tension (dyne/cm): 38.7
5. Polarization rate (10-24cm3): 19.05
Calculate chemical data
1. Reference value for hydrophobic parameter calculation (XlogP): None
2. Number of hydrogen bond donors: 0
3. Number of hydrogen bond acceptors: 2
4. Number of rotatable chemical bonds: 1
5. Number of tautomers: None
6. Topological molecular polarity surface area 12.5
7. Number of heavy atoms: 12
8. Surface charge: 0
9. Complexity: 126
10. Number of isotopic atoms: 0
11. Determine the number of atomic stereocenters: 0
12. Uncertain number of atomic stereocenters: 0
13. Determine the number of chemical bond stereocenters: 0
14. Number of uncertain chemical bond stereocenters: 0
15. Number of covalent bond units: 1
Nature and stability
N-phenylmorpholine is a highly stable compound that is not easily ignited. Chemical property pKa 3.20 (25 ℃, water). Condensation occurs with benzaldehyde to form a colorless matrix, which is then rearranged to obtain a peacock green dye. Due to the presence of the morpholine group, the ortho para position of the benzene ring is activated and reacts with nitric acid to obtain ortho - and para nitro compounds. It is relatively stable to oxidation and only produces a small amount of formaldehyde when oxidized with dichromate.
Storage method
This product should be sealed and stored.
Second, the Synthetic Route we will recommend is the most important for your reference?
First, synthesis line of 4-Phenylmorpholine CAS NO.92-53-5 as follows
Main synthetic method
Prepared by the reaction of N, N-di - β - hydroxyethyl aniline and sulfuric acid.
Refining method: Recrystallize and refine with water.
Third, what is the usage of 4-Phenylmorpholine CAS NO.92-53-5 ? pleas see below
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Usage:
The compound has similar properties to N, N-dimethylaniline, is alkaline, and can be used as a reagent for dehydrobromination of allyl bromide compounds. It has the advantage of easy purification of the product. Used as an anti-corrosion additive, intermediate for dye insecticides, and catalyst for peroxide decomposition.
Other usage:
Used for the synthesis of 2-(N-formylanilino)ethyl formate, Cas no. 13238-43-2
Used for the synthesis of Canthaxanthin, Cas no. 514-78-3
Used for the synthesis of 4-Cyclohexylmorpholine Cas no. 6425-41-8
Besides Safety Information of 4-Phenylmorpholine CAS NO.92-53-5 is also important when handling it
Hazard Codes |
Xi |
WGK Germany |
3 |
H.S.Code: |
2934 9990.99 |
TSCA |
Yes |
HazardClass |
IRRITANT |
What is the appearance of 4-Phenylmorpholine CAS NO.92-53-5? Please see the picture of 4-Phenylmorpholine CAS NO.92-53-5, below
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Specification of 4-Phenylmorpholine CAS NO.92-53-5, is below
Apperance: white to brownish crystalline solid.
Assay: 98 min by GC
IR identity: conform
Melting poing:51-54℃
IR picture of 4-Phenylmorpholine CAS NO.92-53-5 is as follows,
HNMR Spectrum picture of 4-Phenylmorpholine CAS NO.92-53-5 is as follows,
Reference of Article cited for your reference below,
(1)
Publication Name: Catalysis Letters
Publication Date: 2023-08-09
DOI: 10.1007/s10562-023-04432-w
(2)
Can Aphid Herbivory Induce Intergenerational Effects of Endophyte-conferred Resistance in Grasses?
Publication Name: Journal of Chemical Ecology
Publication Date: 2022-11-14
PMID: 36372818
DOI: 10.1007/s10886-022-01390-2
(3)
An updated review on 1,2,3-/1,2,4-triazoles: synthesis and diverse range of biological potential
Publication Name: Molecular Diversity
Publication Date: 2024-07-27
PMID: 39066993
DOI: 10.1007/s11030-024-10858-0