Product Details
Buy high quality and low price N-(2-HYDROXYPROPYL)MORPHOLINE 2109-66-2 now
- Molecular Formula:C7H15NO2
- Molecular Weight:145.202
- Vapor Pressure:0.0102mmHg at 25°C
- Refractive Index:1.4620
- Boiling Point:233.6 °C at 760 mmHg
- PKA:14.95±0.20(Predicted)
- Flash Point:95.1 °C
- PSA：32.70000
- Density:1.033 g/cm3
- LogP:-0.36270
N-(2-HYDROXYPROPYL)MORPHOLINE(Cas 2109-66-2) Usage
InChI:InChI=1/C7H15NO2/c1-7(9)6-8-2-4-10-5-3-8/h7,9H,2-6H2,1H3/t7-/m0/s1
2109-66-2 Relevant articles
Tetranuclear Zn complex covalently immobilized on sulfopropylsilylated mesoporous silica: An efficient catalyst for ring opening reaction of epoxide with amine
Bandyopadhyay, Mahuya,Bandyopadhyay, Rajib,Das, Sourav,Jadav, Divya,Kubota, Yoshihiro,Shukla, Pooja
, (2020)
Tetranuclear Zn complex, [Zn4(L)2(LH)2((...
Micellization and antimicrobial properties of N-alkyl-(2-hydroxypropyl)morpholinium bromides
Ahmadova, Gulnara A.,Huseynova, Khuraman A.,Mammadov, Rustam Kh.,Muradova, Sevda A.,Qasimova, Fatma I.,Rahimov, Ravan A.,Rustamova, Inara V.,Zubkov, Fedor I.
, (2021)
New ionic-liquid cationic surfactants ha...
Tetragonal versus hexagonal: Structure-dependent catalytic activity of Co/Zn bimetallic metal-organic frameworks
Pariyar, Anand,Asl, Hooman Yaghoobnejad,Choudhury, Amitava
supporting information, p. 9250 - 9257 (2016/09/28)
Tetragonal and hexagonal phases of monom...
A solvent free method for preparation of β-amino alcohols by ring opening of epoxides with amines using MCM-22 as a catalyst
Baskaran, Thangaraj,Joshi, Akanksha,Kamalakar, Gunda,Sakthivel, Ayyamperumal
, p. 50 - 55 (2016/07/06)
β-amino alcohols were synthesized at roo...
2109-66-2 Process route
-
-
110-91-8,99108-56-2
morpholine
-
-
75-56-9,16033-71-9
methyloxirane
-
-
2109-66-2
4-(2-hydroxypropyl)morpholine
| Conditions | Yield |
|---|---|
|
In
water;
at 90 ℃;
for 9h;
regioselective reaction;
|
98% |
|
at 20 ℃;
for 48h;
Inert atmosphere;
|
98% |
|
With
bismuth(III) chloride;
In
pentane;
at 20 ℃;
for 24h;
|
97% |
|
In
water;
at 0 - 20 ℃;
|
93% |
|
scandium tris(trifluoromethanesulfonate);
at 20 ℃;
for 12h;
|
88% |
|
1,3-bis(3,5-bis(trifluoro-ethyl)phenyl)thiourea;
In
water;
at 20 ℃;
for 36h;
|
83% |
|
With
methanol;
|
|
|
Heating;
|
|
|
With
2.5Zn(2+)*0.5Co(2+)*O(2-)*1.667C9H3O6(3-)*3C3H7NO*0.667H2O*H(1+)*0.33C2H7N;
In
neat (no solvent);
at 40 ℃;
for 14h;
Reagent/catalyst;
chemoselective reaction;
Molecular sieve;
Sealed tube;
|
99 %Spectr. |
-
-
110-91-8,99108-56-2
morpholine
-
-
75-56-9,16033-71-9
methyloxirane
-
-
69296-06-6
beta-methyl morpholinoethanol
-
-
2109-66-2
4-(2-hydroxypropyl)morpholine
| Conditions | Yield |
|---|---|
|
In
methanol;
at 45 ℃;
for 3h;
Yield given. Yields of byproduct given. Title compound not separated from byproducts;
|
|
|
With
Na-MCM-22 zeolite;
In
neat (no solvent);
at 35 ℃;
for 6h;
Overall yield = 59 %;
Green chemistry;
|
|
|
With
tetranuclear zinc(II) complex covalently immobilized on sulfopropylsilylated mesoporous silica catalyst;
In
neat (no solvent);
at 70 ℃;
Catalytic behavior;
|
2109-66-2 Upstream products
-
110-91-8
morpholine
-
127-00-4
1-Chloro-2-propanol
-
78-96-6
3-amino-2-propanol
-
111-44-4
3-oxa-1,5-dichloropentane
2109-66-2 Downstream products
-
54504-91-5
hydroxy-diphenyl-acetic acid 1-methyl-2-morpholin-4-yl-ethyl ester
-
6425-39-4
2,2'-dimorpholinodiethyl ether
-
111681-72-2
alpha-methyl-bis<2(4-morpholino)ethyl> ether
-
111692-76-3
4-[2-[2-(4-morpholinyl)-1-methylethoxy]-ethyl]-2,6-dimethylmorpholine
N-(2-HYDROXYPROPYL)MORPHOLINE
CAS:2109-66-2
Purity:99%
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