- Chemical Name: 3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER
- CAS No.: 21911-84-2
Quality products?make an important contribution to long-term revenue and profitability. Factory Sells Best Quality 3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER 21911-84-2 with GMP standards
1.What is the 3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER ?
Used in Pharmaceutical Industry:
3-Phenylamino-propionic acid methyl ester is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structure allows for the creation of a diverse range of medicinal compounds, enhancing the therapeutic potential of pharmaceutical products.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 3-Phenylamino-propionic acid methyl ester serves as a versatile building block for the synthesis of other organic compounds. Its reactivity and functional groups make it suitable for a wide array of chemical reactions, contributing to the advancement of organic chemistry research and the creation of novel organic materials.
Used in Research and Development:
3-Phenylamino-propionic acid methyl ester is employed as a crucial component in the research and development of new drugs. Its presence in laboratory settings facilitates the exploration of its chemical properties and potential applications, driving innovation in the pharmaceutical and chemical industries.
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292638-85-8,9003-21-8,96-33-3
acrylic acid methyl ester
-
-
62-53-3
aniline
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![methyl 3-[(3-methoxy-3-oxopropyl)anilino]propanoate](/upload/2026/8/aba889f233784df48538f33c6217920b_39686179-588c-42d4-a9d9-9eb32b789906.png)
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53733-94-1
methyl 3-[(3-methoxy-3-oxopropyl)anilino]propanoate
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21911-84-2
methyl 3-(phenylamino)propanoate
| Conditions | Yield |
|---|---|
|
With
aluminum oxide;
at 100 - 110 ℃;
for 3h;
|
97%
1% |
|
In
2,2,2-trifluoroethanol; water;
at 80 ℃;
for 16h;
|
94 %Spectr.
6 %Spectr. |
-
-
292638-85-8,9003-21-8,96-33-3
acrylic acid methyl ester
-
-
62-53-3
aniline
-
-
21911-84-2
methyl 3-(phenylamino)propanoate
| Conditions | Yield |
|---|---|
|
With
silica-supported aluminum chloride;
at 60 ℃;
for 4h;
Neat (no solvent);
|
100%
|
|
With
acetic acid;
at 25 - 70 ℃;
for 4h;
|
99%
|
|
With
nickel(II) ferrite;
In
water;
at 100 ℃;
Green chemistry;
|
98%
|
|
With
triethylammonium acetate;
at 25 ℃;
for 0.3h;
chemoselective reaction;
|
96%
|
|
With
ionic liquid [bmim]BF4 stabilized magnetic cobalt nanoparticles;
In
neat (no solvent);
at 20 ℃;
for 0.75h;
|
94%
|
|
With
Ps-AlCl3;
at 70 ℃;
for 2.5h;
Temperature;
Time;
Reagent/catalyst;
Solvent;
chemoselective reaction;
|
93%
|
|
With
glutathione-modified ferrite nanoparticles;
In
water;
at 140 ℃;
for 0.333333h;
under 2585.81 - 9308.91 Torr;
Microwave irradiation;
|
92%
|
|
With
OMS-MIL-100(Fe);
In
toluene;
at 50 ℃;
for 24h;
Solvent;
Reagent/catalyst;
Sealed tube;
Schlenk technique;
Green chemistry;
|
92%
|
|
With
ruthenium trichloride;
In
PEG 2000;
at 20 ℃;
for 15h;
|
91%
|
|
With
lithium tetrafluoroborate;
at 70 ℃;
for 0.25h;
Neat (no solvent);
|
90%
|
|
With
1-methyl-1H-imidazolium trifluoroacetate;
at 80 ℃;
for 4h;
|
90%
|
|
fipronilβ-cyclodextrin;
In
water; acetone;
at 20 ℃;
for 8h;
|
88%
|
|
With
3-(N,N-dimethyldodecylammonium)propanesulfonic acid hydrogen sulphate;
In
water;
at 20 ℃;
for 4h;
|
88%
|
|
With
N,N,N-trimethyl-N-(propanesulfonic acid)ammonium hydrogensulfate;
In
water;
at 20 ℃;
for 4h;
|
88%
|
|
With
Zeolite NaY;
In
neat (no solvent);
Microwave irradiation;
|
88%
|
|
With
Imidazole hydrochloride;
In
neat (no solvent);
at 100 ℃;
for 2h;
Green chemistry;
|
88%
|
|
With
acetic acid;
for 15h;
Heating;
|
85%
|
|
With
polyacrylamide coated magnetite (PAM(at)MNP);
In
neat (no solvent);
at 65 ℃;
for 4h;
Temperature;
Reagent/catalyst;
Solvent;
|
85%
|
|
With
trifluorormethanesulfonic acid;
In
toluene;
at 30 ℃;
for 4h;
Reagent/catalyst;
Solvent;
Temperature;
|
83%
|
|
With
acetic acid;
at 170 ℃;
for 0.5h;
microwave irradiation;
|
82%
|
|
With
phosphotungstic acid;
In
water;
at 20 ℃;
for 40h;
|
82%
|
|
With
acetic acid;
at 200 ℃;
for 0.333333h;
Microwave irradiation;
|
81%
|
|
With
acetic acid;
at 20 - 200 ℃;
for 0.333333h;
|
78%
|
|
With
boric acid; glycerol;
In
water;
at 100 ℃;
for 18h;
Green chemistry;
|
78%
|
|
With
acetic acid;
for 15h;
Inert atmosphere;
Reflux;
|
72%
|
|
With
iodine;
In
toluene;
at 110 ℃;
for 7h;
|
70%
|
|
aniline;
With
potassium tert-butylate; copper(l) chloride; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride;
In
toluene;
for 0.333333h;
Inert atmosphere;
acrylic acid methyl ester;
In
toluene;
at 22 ℃;
for 15h;
Inert atmosphere;
|
70%
|
|
With
acetic acid;
at 25 - 70 ℃;
for 4h;
|
65%
|
|
[(dppf)Pd(NCMe)(H2O)](OTf)2;
In
toluene;
at 100 ℃;
for 18h;
|
64%
|
|
With
aluminum oxide;
at 20 ℃;
for 8h;
Neat (no solvent);
|
63%
|
|
With
indium(III) chloride;
In
water;
1.) r.t., 10 min, 2.) r.t., 18 h;
|
45%
|
|
In
water;
at 50 ℃;
for 24h;
|
35%
|
|
acrylic acid methyl ester; aniline;
In
water;
at 80 ℃;
for 16h;
|
34%
|
|
With
lithium perchlorate;
at 20 ℃;
for 4h;
|
30%
|
|
With
ZrOCl2*8H2O on montmorillonite K10;
at 20 ℃;
for 3h;
|
29%
|
|
With
1,8-diazabicyclo[5.4.0]undec-7-ene;
In
acetonitrile;
at 20 ℃;
for 48h;
|
24%
|
|
With
acetic acid;
at 79 ℃;
|
12%
|
|
With
1,1,3,3-tetramethylguanidinium lactate;
at 20 ℃;
for 24h;
Neat (no solvent);
|
12%
|
|
With
acetic acid;
|
|
|
With
acetic acid; hydroquinone;
|
|
|
With
sodium hydroxide; sodium tetrahydroborate; mercury(II) diacetate;
Yield given. Multistep reaction;
1.) THF, 5 h, 2.) 15 h;
|
|
|
With
acetic acid;
for 22h;
Heating;
|
|
|
With
[(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)Cu(I)(anilido)];
In
benzene-d6;
at 20 ℃;
for 19h;
|
55 % Spectr.
|
|
With
tetrabutylammonium acetate; acetic acid;
at 200 ℃;
for 0.333333h;
microwave irradiation;
|
|
|
polystyrenesulfonic acid;
In
water;
at 80 ℃;
under 2068.65 - 3620.13 Torr;
microwave irradiation;
|
95 % Chromat.
|
|
With
acetic acid;
at 200 ℃;
for 0.333333h;
Microwave irradiation;
Combinatorial reaction / High throughput screening (HTS);
|
73 %Spectr.
|
|
With
tetrachlorosilane;
at 0 - 60 ℃;
Inert atmosphere;
neat (no solvent);
|
|
|
With
Candida antarctica lipase B;
In
toluene;
at 60 ℃;
for 42h;
|
31 %Chromat.
|
|
With
squaric acid;
In
water;
at 20 ℃;
for 8h;
|
90 %Spectr.
|
|
With
Zr-nano(propyltriethoxysilane)-ZSM-5 (50);
at 79.84 ℃;
for 12h;
Catalytic behavior;
|
|
|
With
C34H42F6N4O6S2Zr;
In
benzene-d6;
at 20 ℃;
for 1h;
Time;
Catalytic behavior;
Inert atmosphere;
Schlenk technique;
Glovebox;
|
75 %Spectr.
|
|
With
Pseudomonas fluorescence lipase immobilized on hyroxypropyl methyl cellulose support;
In
toluene;
at 50 ℃;
for 3h;
Reagent/catalyst;
chemoselective reaction;
Enzymatic reaction;
|
|
|
In
toluene;
Reflux;
|
|
|
With
C12H27N*AlCl3;
In
water;
at 25 ℃;
for 0.5h;
Green chemistry;
|
92 %Chromat.
|
|
With
nano copper(0) complex supported on pandanus nanocellulose;
In
ethanol;
at 20 ℃;
for 4h;
|
94 %Chromat.
|
|
With
aluminum (III) chloride;
In
neat (no solvent);
at 60 ℃;
for 4h;
Inert atmosphere;
|
2.What is the CAS number for 3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER ?
The CAS number of 3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER is 21911-84-2.
More information of 3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER 21911-84-2 are:
|
CAS?Number |
21911-84-2 |
|
Density |
1.107 g/cm3 |
|
Boiling Point |
308.334 °C at 760 mmHg |
|
Flash Point |
140.276 °C |
|
HS CODE |
2922499990 |
|
PSA |
38.33000 |
|
LogP |
1.73460 |
3.What are another words for 3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER ?
Synonyms?for?3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER 21911-84-2:3-(Phenylamino)propanoicacid methyl ester;Methyl 3-(N-Phenylamino)propionate;Methyl3-(phenylamino)propanoate;Methyl 3-anilinopropionate;Methyl b-(N-phenyl)aminopropionate;Methyl b-anilinopropionate;N-[(Methoxycarbonyl)ethyl]aniline;N-[2-(Methoxycarbonyl)ethyl]aniline;NSC144467;
4.What is the molecular formula of 3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER?
The chemical formula of ?3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER is?C10H13NO2 which containing 10 Carbon atoms,13 Hydrogen atoms,1 Nitrogen atoms and 2 Oxygen atoms,and the molecular weight of??3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER?is 179.219.
5.What is 3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER (21911-84-2) used for?
3-Phenylamino-propionic acid methyl ester, with the molecular formula C11H15NO2, is a methyl ester derivative of 3-phenylamino-propionic acid. It is an organic compound characterized by the presence of a phenyl group attached to an amino-propionic acid molecule and a methyl ester group. This chemical is widely utilized in the synthesis of pharmaceuticals and other organic compounds, making it a valuable intermediate in the development of new drugs and a common component in various laboratory settings.
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6.Buy 3-PHENYLAMINO-PROPIONIC ACID METHYL ESTER with the best price .
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