H-4-NITRO-PHE-OET HCL
- CAS: 58816-66-3
- Purity: 99%
- Manufacturer supply good quality H-4-NITRO-PHE-OET HCL 58816-66-3 with stock
Manufacturer supply good quality H-4-NITRO-PHE-OET HCL 58816-66-3 with stock
- Molecular Formula: C11H15ClN2O4
- Molecular Weight: 274.704
- Vapor Pressure: 9.83E-06mmHg at 25°C
- Melting Point: 177-180 °C
- Refractive Index: 1.556
- Boiling Point: 372.1 °C at 760 mmHg
- Flash Point: 178.9 °C
- PSA： 98.14000
- Density: 1.246 g/cm3
- LogP: 3.05320
H-4-NITRO-PHE-OET HCL(Cas 58816-66-3) Usage
|
General Description |
H-4-NITRO-PHE-OET HCL, also known as 4-nitrophenyl ethyl ether hydrochloride, is a chemical compound used in the synthesis of pharmaceuticals, agrochemicals, and organic compounds. It is a nitrophenyl ether derivative, which contains a nitro group and an ether functional group. H-4-NITRO-PHE-OET HCL is used as a reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-oxygen bonds. It is also used as a building block in the preparation of various biologically active compounds and in the development of new medicinal products. Additionally, it is utilized as a chemical intermediate in the production of dyes, polymers, and other organic materials. |
InChI:InChI=1/C11H14N2O4/c1-2-17-11(14)10(12)7-8-3-5-9(6-4-8)13(15)16/h3-6,10H,2,7,12H2,1H3/t10-/m0/s1
58816-66-3 Relevant articles
A PROCESS FOR THE SYNTHESIS OF MELPHALAN
-
Page/Page column 13, (2021/07/02)
The invention relates to a process for t...
Tuning the reaction pathways of phenanthroline-Schiff bases: Routes to novel phenanthroline ligands
Ahmed, Muhib,Rooney, Denise,McCann, Malachy,Casey, Jamie,O'Shea, Katie,Twamley, Brendan
, p. 15283 - 15289 (2019/10/22)
Pyrido-phenanthrolin-7-one compounds are...
VLA-4 ANTAGONISTS
-
Page/Page column 17, (2008/06/13)
Substituted N-[N-(sulphonylphenyl)sulfon...
VLA-4 ANTAGONISTS
-
Page/Page column 18, (2008/06/13)
Compounds of Formula I are antagonists o...
58816-66-3 Process route
-
-
64-17-5
ethanol
-
-
949-99-5
4-nitro-3-phenyl-L-alanine
-
-
58816-66-3
(S)-2-amino-3-(4-nitrophenyl)propionic acid ethyl ester hydrochloride
| Conditions | Yield |
|---|---|
|
With
thionyl chloride;
at 0 - 80 ℃;
for 4h;
|
95%
|
|
With
thionyl chloride;
at 0 - 20 ℃;
Heating / reflux;
|
|
|
With
acetyl chloride;
for 3h;
Reflux;
|
-
-
949-99-5
4-nitro-3-phenyl-L-alanine
-
-
58816-66-3
(S)-2-amino-3-(4-nitrophenyl)propionic acid ethyl ester hydrochloride
| Conditions | Yield |
|---|---|
|
ethanol;
With
thionyl chloride;
at 0 - 20 ℃;
for 0.75h;
4-nitro-3-phenyl-L-alanine;
Heating / reflux;
|
92%
|
58816-66-3 Upstream products
-
64-17-5
ethanol
-
949-99-5
4-nitro-3-phenyl-L-alanine
58816-66-3 Downstream products
-
36097-40-2
(S)-ethyl 2-acetamido-3-(4-nitrophenyl)propanoate
-
67630-00-6
N-(tert-butyloxycarbonyl)-4-nitro-L-phenylalanine ethyl ester
-
67630-01-7
(S)-3-(4-aminophenyl)-2-tert-butoxycarbonylamino-propionic acid ethyl ester
-
189744-27-2
N-boc-L-3-(4-bis(hydroxyethyl)aminophenyl)alanine ethyl ester
Leave Your Message
Related Products
