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Manufacturer supply 2,4-Dichloro-6-methoxy-1,3,5-triazine 3638-04-8 with sufficient stock and high standard
- Molecular Formula: C4H3Cl2N3O
- Molecular Weight: 179.993
- Appearance/Colour: WHITE POWDER OR CRYSTALS
- Vapor Pressure: 0.00022mmHg at 25°C
- Melting Point: 86-88 °C(lit.)
- Refractive Index: 1.545
- Boiling Point: 336.3 °C at 760 mmHg
- PKA: -1.40±0.10(Predicted)
- Flash Point: 157.2 °C
- PSA： 47.90000
- Density: 1.538 g/cm3
- LogP: 1.18700
2,4-Dichloro-6-methoxy-1,3,5-triazine(Cas 3638-04-8) Usage
InChI:InChI=1/C4H3Cl2N3O/c1-10-4-8-2(5)7-3(6)9-4/h1H3
3638-04-8 Relevant articles
Synthesis and characterization of lanthanide complexes with a pentadentate triazine-based ligand
Pavelek, Lubomír,Ladányi, Vít,Ne?as, Marek,Moravec, Zdeněk,Wichterle, Kamil
, p. 134 - 141 (2016)
A series of mononuclear [Ln(L)(H2O)(NO3)...
Synthesis and antiproliferating activity of iron chelators of hydroxyamino-1,3,5-triazine family
Sun, Daekyu,Melman, Galina,LeTourneau, Nickolas J.,Hays, Allison M.,Melman, Artem
, p. 458 - 460 (2010)
We synthesized and evaluated new specifi...
Inhibition of acetolactate synthase isozyme II from Escherichia coli by a new azido-photoaffinity sulfonylurea
Ortega, Florence,Bastide, Jean
, p. 261 - 274 (1997)
The sulfonylurea herbicides are very pat...
Triazine based Mn (II) and Mn (II)/Ln (III) complexes: Synthesis, characterization and catecholase activities
Celik, Derya,Kose, Muhammet
, (2019)
In the current work, two triazine-based ...
A highly emissive fluorescent Zn-MOF: molecular decoding strategies for solvents and trace detection of dunnite in water
Das, Prasenjit,Mandal, Sanjay K.
, p. 21274 - 21279 (2018)
The strategic exploration of a highly em...
Two heptacoordinated manganese(II) complexes of giant pentadentate s-triazine bis-Schiff base ligand: Synthesis, crystal structure, biological and DFT studies
Soliman, Saied M.,El-Faham, Ayman,Elsilk, Sobhy E.,Farooq, Muhammad
, p. 275 - 285 (2018)
A new s-triazine bis-Schiff base chelati...
Synthesis of Amidation Agents and Their Reactivity in Condensation Reactions
Sole, Roberto,Agostinis, Lodovico,Conca, Silvia,Gatto, Vanessa,Bardella, Noemi,Morandini, Andrea,Buranello, Chiara,Beghetto, Valentina
supporting information, p. 1672 - 1682 (2021/02/01)
Nowadays, the development of new approac...
Synthesis and Antimicrobial Evaluation of Bis-morpholine Triazine Quaternary Ammonium Salts
Morandini, Andrea,Leonetti, Benedetta,Riello, Pietro,Sole, Roberto,Gatto, Vanessa,Caligiuri, Isabella,Rizzolio, Flavio,Beghetto, Valentina
supporting information, p. 3172 - 3176 (2021/08/03)
Efficient, environmentally and economica...
Interfering with the Tumor-Immune Interface: Making Way for Triazine-Based Small Molecules as Novel PD-L1 Inhibitors
Russomanno, Pasquale,Assoni, Giulia,Amato, Jussara,D'Amore, Vincenzo Maria,Scaglia, Riccardo,Brancaccio, Diego,Pedrini, Martina,Polcaro, Giovanna,La Pietra, Valeria,Orlando, Paolo,Falzoni, Marianna,Cerofolini, Linda,Giuntini, Stefano,Fragai, Marco,Pagano, Bruno,Donati, Greta,Novellino, Ettore,Quintavalle, Cristina,Condorelli, Gerolama,Sabbatino, Francesco,Seneci, Pierfausto,Arosio, Daniela,Pepe, Stefano,Marinelli, Luciana
, p. 16020 - 16045 (2021/11/10)
The inhibition of the PD-1/PD-L1 axis by...
Synthesis and kinetic study of a series of chloro- and m-carboxypyridium triazinyl reactive dyes
Huang, Huei-Chin,Wu, Chun-Guey
, (2021/02/12)
Five monochloro-s-triazinyl reactive dye...
3638-04-8 Process route
-
-
67-56-1
methanol
-
-
108-77-0
1,3,5-trichloro-2,4,6-triazine
-
-
3638-04-8
2,4-Dichloro-6-methoxy-1,3,5-triazine
Conditions
| Conditions | Yield |
|---|---|
|
With
sodium hydrogencarbonate;
In
water;
at 0 ℃;
for 2.5h;
|
98%
|
|
With
sodium hydrogencarbonate;
at 20 ℃;
for 0.5h;
|
98%
|
|
With
sodium hydrogencarbonate;
at 25 ℃;
for 0.5h;
|
98%
|
|
With
sodium hydrogencarbonate;
at 0 ℃;
for 1h;
|
97%
|
|
With
sodium hydrogencarbonate;
at 0 ℃;
for 1h;
|
97%
|
|
With
sodium hydrogencarbonate;
In
water;
at 20 - 30 ℃;
|
86.2%
|
|
With
sodium hydrogencarbonate;
In
water;
at 20 - 30 ℃;
|
86.2%
|
|
With
sodium hydrogencarbonate;
In
water;
at 20 - 30 ℃;
for 0.5h;
|
86.2%
|
|
methanol;
With
sodium hydrogencarbonate;
In
water;
at 20 ℃;
1,3,5-trichloro-2,4,6-triazine;
In
water;
at 30 ℃;
for 0.5h;
|
86.2%
|
|
With
sodium hydrogencarbonate;
In
water;
at 20 - 30 ℃;
|
86.2%
|
|
With
sodium hydrogencarbonate;
In
water;
at 20 - 30 ℃;
for 0.5h;
|
86.2%
|
|
With
sodium hydrogencarbonate;
at 10 - 20 ℃;
for 1h;
|
85%
|
|
With
sodium hydrogencarbonate;
In
water;
at 30 ℃;
for 0.5h;
|
84%
|
|
With
sodium hydrogencarbonate;
In
water;
at 20 ℃;
for 1h;
|
83%
|
|
With
sodium hydrogencarbonate;
at 0 - 20 ℃;
|
82%
|
|
With
sodium hydrogencarbonate;
at 0 - 20 ℃;
for 2h;
|
82%
|
|
With
sodium hydrogencarbonate;
In
water;
at 0 - 20 ℃;
for 0.5h;
|
80%
|
|
methanol; 1,3,5-trichloro-2,4,6-triazine;
In
water; acetone;
for 0.333333h;
With
potassium carbonate;
In
water; acetone;
at 0 ℃;
for 2h;
|
76.3%
|
|
With
sodium hydrogencarbonate;
at 0 ℃;
for 0.333333h;
|
74%
|
|
With
sodium hydrogencarbonate;
at 0 ℃;
for 0.333333h;
|
74%
|
|
With
sodium hydrogencarbonate;
In
dichloromethane;
at 20 ℃;
for 0.5h;
Inert atmosphere;
|
73%
|
|
With
sodium hydrogencarbonate;
In
water;
at 30 ℃;
|
67%
|
|
With
sodium hydrogencarbonate;
for 1h;
Ambient temperature;
|
60%
|
|
With
sodium hydrogencarbonate;
at 0 - 10 ℃;
for 1h;
|
57.8%
|
|
With
sodium hydrogencarbonate;
at 20 ℃;
|
55.1%
|
|
With
sodium hydrogencarbonate;
In
water;
at 0 - 20 ℃;
for 0.5h;
|
50%
|
|
With
2,4,6-trimethyl-pyridine;
|
|
|
With
sodium hydrogencarbonate;
|
|
|
With
sodium hydrogencarbonate;
|
|
|
With
ISOPROPYLAMIDE;
In
acetone;
at 35 ℃;
for 2.5h;
Yield given;
|
|
|
With
sodium hydrogencarbonate;
at 20 ℃;
for 0.5h;
|
|
|
With
sodium hydrogencarbonate;
at 30 ℃;
|
|
|
In
water;
at 0 - 10 ℃;
pH=6;
|
|
|
With
2,6-dimethylpyridine;
In
acetone;
at -2 - 20 ℃;
|
|
|
With
sodium hydrogencarbonate;
at 0 ℃;
for 5h;
|
|
|
With
sodium hydrogencarbonate;
at 20 ℃;
for 0.75h;
|
|
|
With
sodium hydrogencarbonate;
at 20 ℃;
for 1h;
|
|
|
With
sodium hydrogencarbonate;
at 10 - 20 ℃;
for 1h;
|
|
|
With
sodium hydrogencarbonate;
at 130 ℃;
for 1h;
|
|
|
With
sodium hydrogencarbonate;
at 0 ℃;
|
|
|
With
sodium hydrogencarbonate;
at 0 ℃;
for 10h;
|
|
|
With
sodium hydrogencarbonate;
In
water; acetone;
at 0 - 5 ℃;
|
|
|
With
pyrrolidine;
at 0 ℃;
for 1h;
|
|
|
With
sodium hydrogencarbonate;
|
|
|
With
sodium hydrogencarbonate;
at 10 - 25 ℃;
|
-
-
108-77-0
1,3,5-trichloro-2,4,6-triazine
-
-
3638-04-8
2,4-Dichloro-6-methoxy-1,3,5-triazine
Conditions
| Conditions | Yield |
|---|---|
|
With
sodium hydrogencarbonate;
In
methanol; (2S)-N-methyl-1-phenylpropan-2-amine hydrate;
|
|
|
With
sodium hydrogencarbonate;
In
methanol; water;
|
3638-04-8 Upstream products
-
67-56-1
methanol
-
108-77-0
1,3,5-trichloro-2,4,6-triazine
-
124-41-4
sodium methylate
-
108-98-5
thiophenol
3638-04-8 Downstream products
-
14925-07-6
2,4-bis-aziridin-1-yl-6-methoxy-[1,3,5]triazine
-
3140-73-6
2-chloro-4,6-dimethoxy-1 ,3,5-triazine
-
140452-00-2
2,4-dibenzoyloxy-6-methoxy-1,3,5-triazine
-
108718-58-7
2-methoxy-4,6-diphenyl-1,3,5-triazine
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