- CAS
- Purity
- 2696-85-7
- 99%
Chinese factory supply 2-N-BUTYLANILINE 2696-85-7 in stock with high standard
- Molecular Formula: C10H15 N
- Molecular Weight: 149.236
- Vapor Pressure: 0.0235mmHg at 25°C
- Refractive Index: 1.5360-1.5390
- Boiling Point: 249°Cat760mmHg
- PKA: 4.27±0.10(Predicted)
- Flash Point: 105.4°C
- PSA： 26.02000
- Density: 0.947g/cm3
- LogP: 3.19260
2-N-BUTYLANILINE(Cas 2696-85-7) Usage
|
General Description |
2-N-BUTYLANILINE is a chemical compound with the molecular formula C10H15N. It is a pale yellow liquid with a faint amine odor. It is primarily used as an intermediate in the production of various dyes and pigments, as well as in the synthesis of organic compounds. It is also utilized as a corrosion inhibitor in metalworking fluids, and as a stabilizer for polymers and fuels. In addition, 2-N-BUTYLANILINE has been found to possess potential antioxidant properties, making it useful in the formulation of antioxidant additives for various industrial applications. However, it is important to handle this chemical with care as it can be harmful if ingested, inhaled, or if it comes into contact with the skin. |
InChI:InChI=1/C10H15N/c1-2-3-6-9-7-4-5-8-10(9)11/h4-5,7-8H,2-3,6,11H2,1H3
2696-85-7 Relevant articles
-
Gassman,Gruetzmacher
, p. 588 (1973)
-
Ligand assessment for the suzuki-miyaura cross coupling reaction of aryl and heteroaryl bromides with n-butylboronic acid. The advantages of buchwald's s-phos
Jagusch, Thomas,Lehnemann, Bernd,Meudt, Andreas,Nerdinger, Sven,Neuner, Sandro,Scherer, Stefan,Schottenberger, Herwig,Snieckus, Victor
, p. 631 - 644 (2020/01/31)
An investigation of biarylphosphine liga...
Structural development of liver X receptor (LXR) antagonists derived from thalidomide-related glucosidase inhibitors
Noguchi-Yachide, Tomomi,Miyachi, Hiroyuki,Aoyama, Hiroshi,Aoyama, Atsushi,Makishima, Makoto,Hashimoto, Yuichi
, p. 1750 - 1754 (2008/09/17)
Following our previous discovery of LXR ...
Synthesis of enantiopure 1-aryl-1-butylamines and 1-aryl-3-butenylamines by diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine amide
Dalmolen, Jan,Van Der Sluis, Marcel,Nieuwenhuijzen, Jose W.,Meetsma, Auke,De Lange, Ben,Kaptein, Bernard,Kellogg, Richard M.,Broxterman, Quirinus B.
, p. 1544 - 1557 (2007/10/03)
The synthesis of enantiopure 1-aryl-1-bu...
Para-bromination of ortho-alkyl anilines
-
, (2008/06/13)
A process of selectively preparing p-bro...
2696-85-7 Process route
-
-
4426-47-5
butylboronic acid
-
-
615-36-1
2-bromoaniline
-
-
2696-85-7
2-butyl-benzenamine
Conditions
| Conditions | Yield |
|---|---|
|
With
dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate; potassium carbonate; caesium carbonate;
In
toluene;
at 80 ℃;
for 16h;
Inert atmosphere;
|
64%
|
-
-
50461-36-4
2-(o-aminophenyl)tetrahydrothiophen
-
-
2696-85-7
2-butyl-benzenamine
Conditions
| Conditions | Yield |
|---|---|
|
|
62%
|
2696-85-7 Upstream products
-
91-63-4
2-methylquinoline
-
7137-55-5
1-butyl-2-nitrobenzene
-
62723-78-8
2-methoxymethylaniline
-
927-77-5
n-propylmagnesium bromide
2696-85-7 Downstream products
-
100861-48-1
1-(2-butyl-phenyl)-piperazine
-
58928-63-5
(o-butylphenyl)hydrazine
-
61653-36-9
1,2-Bis(2-butylphenyl)diazene
-
146509-70-8
di(4-amino-3-n-butylphenyl)acetic acid