119192-10-8
- Product Name:4-(1H-1,2,4-triazol-1-ylmethyl)-Benzenamine
- Molecular Formula:C9H10N4
- Purity:99%
- Molecular Weight:174.205
Product Details;
CasNo: 119192-10-8
Molecular Formula: C9H10N4
Appearance: Brown solid
Buy High Grade Top Purity 4-(1H-1,2,4-triazol-1-ylmethyl)-Benzenamine 119192-10-8 In Bulk Supply
- Molecular Formula:C9H10N4
- Molecular Weight:174.205
- Appearance/Colour:Brown solid
- Vapor Pressure:1.12E-06mmHg at 25°C
- Melting Point:124 °C
- Refractive Index:1.663
- Boiling Point:402.1 °C at 760 mmHg
- PKA:4.42±0.10(Predicted)
- Flash Point:197 °C
- PSA:56.73000
- Density:1.26 g/cm3
- LogP:1.48980
4-(1H-1,2,4-Triazol-1-ylmethyl)aniline(Cas 119192-10-8) Usage
Chemical Properties |
Brown Solid |
Uses |
Rizatriptan intermediate |
InChI:InChI=1/C9H10N4/c10-9-3-1-8(2-4-9)5-13-7-11-6-12-13/h1-4,6-7H,5,10H2
119192-10-8 Relevant articles
High Turnover Pd/C Catalyst for Nitro Group Reductions in Water. One-Pot Sequences and Syntheses of Pharmaceutical Intermediates
Gallou, Fabrice,Li, Xiaohan,Lipshutz, Bruce H.,Takale, Balaram S.,Thakore, Ruchita R.
supporting information, p. 8114 - 8118 (2021/10/25)
Commercially available Pd/C can be used ...
“TPG-lite”: A new, simplified “designer” surfactant for general use in synthesis under micellar catalysis conditions in recyclable water
Thakore, Ruchita R.,Takale, Balaram S.,Hu, Yuting,Ramer, Selene,Kostal, Jakub,Gallou, Fabrice,Lipshutz, Bruce H.
, (2021/04/22)
Using the oxidized, carboxylic acid-cont...
PROCESS FOR THE LARGE SCALE PRODUCTION OF RIZATRIPTAN BENZOATE
-
Page/Page column 4; 8-9, (2008/06/13)
The present invention provides a method ...
IMIDAZOQUINOLINES AS LIPID KINASE INHIBITORS
-
Page/Page column 92, (2008/06/13)
The invention relates to novel organic c...
119192-10-8 Process route
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142-04-1,36663-09-9
aniline hydrochloride
-
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74205-82-6
1-(hydroxymethyl)-1,2,4-triazole
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-
101-77-9
4,4'-diamino diphenyl methane
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-
119192-10-8
4-(1H-1,2,4-triazol-1-ylmethyl)aniline
Conditions | Yield |
---|---|
With
acetic acid;
for 0.0833333h;
Heating;
|
59% 10% |
-
-
6085-99-0
4-amino-1-(4-nitrobenzyl)-1,2,4-triazolium bromide
-
-
119192-10-8
4-(1H-1,2,4-triazol-1-ylmethyl)aniline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps
1: 65 percent / 10percent aq NaNO2 / aq. HCl / 0 °C
2: 80 percent / H2 / 10percent Pd-C / ethyl acetate / 60 °C / 760 Torr
With
hydrogen; sodium nitrite;
palladium on activated charcoal;
In
hydrogenchloride; ethyl acetate;
|
119192-10-8 Upstream products
-
1-(4-nitrophenyl)methyl-1,2,4-triazole
-
aniline hydrochloride
-
1-(hydroxymethyl)-1,2,4-triazole
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4-nitrobenzyl chloride
119192-10-8 Downstream products
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N-(4-fluorobenzal)-4-(1H-1,2,4-triazol-1-ylmethyl)benzeneamine
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N-(4-nitrobenzal)-4-(1H-1,2,4-triazol-1-ylmethyl)benzeneamine
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N-(2,4-dichlorobenzal)-4-(1H-1,2,4-triazol-1-ylmethyl)benzeneamine
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4-((1H-1,2,4-triazol-1-yl)methyl)-2-iodobenzenamine
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-
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