4-tert-Butylbenzylamine
- Name 4-tert-Butylbenzylamine
- CAS 39895-55-1
- Purity 99%
Product Details
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1.What is the 4-tert-Butylbenzylamine ?
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.
-
-
939-97-9
4-tert-Butylbenzaldehyde
-
-
39895-55-1
4-(1,1-dimethylethyl)-benzenemethanamine
| Conditions | Yield |
|---|---|
|
With
nickel(II) tetrafluoroborate hexahydrate; ammonia; hydrogen; bis(2-diphenylphosphinoethyl)phenylphosphine;
In
2,2,2-trifluoroethanol;
at 100 ℃;
for 24h;
chemoselective reaction;
|
92%
|
|
With
N,N'-bis(salicylidene)-1,2-phenylene-diaminocobalt(II); ammonia; hydrogen;
In
water;
at 130 ℃;
for 24h;
Autoclave;
|
91%
|
|
4-tert-Butylbenzaldehyde;
With
Rink resin; trimethyl orthoformate;
at 25 ℃;
for 2h;
With
lithium borohydride;
In
tetrahydrofuran;
at 65 ℃;
for 5h;
With
trifluoroacetic acid;
In
dichloromethane;
at 25 ℃;
|
|
|
With
ammonia; hydrogen;
In
tert-butyl alcohol;
at 120 ℃;
for 24h;
Autoclave;
High pressure;
|
95 %Chromat.
|
-
-
4210-32-6
4-tert-butyl benzonitrile
-
-
39895-55-1
4-(1,1-dimethylethyl)-benzenemethanamine
| Conditions | Yield |
|---|---|
|
With
[Ru(H)(BH4)(CO)(PPh3)(3-(di-tert-butylphosphino)-N-((1-methyl-1H-imidazol-2 yl)methyl)propylamine)]; hydrogen;
In
isopropyl alcohol;
at 50 ℃;
for 3h;
Inert atmosphere;
Autoclave;
|
99%
|
|
With
borane-ammonia complex; C15H30Cl2CoN3P;
In
hexane;
at 50 ℃;
for 16h;
chemoselective reaction;
Sealed tube;
Inert atmosphere;
|
80%
|
|
With
[bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); {[(phenylphosphinediyl)bis(2,1-phenylene)]bis(methylene)}bis(di-tert-butylphosphine); hydrogen;
In
isopropyl alcohol;
at 50 ℃;
for 17h;
under 11251.1 Torr;
Inert atmosphere;
Autoclave;
|
90 %Chromat.
|
|
4-tert-butyl benzonitrile;
With
cobalt(III) acetylacetonate; tris(2-(dicyclohexylphosphanyl)ethyl)phosphane;
In
tert-butyl alcohol;
Sealed tube;
Inert atmosphere;
With
potassium tert-butylate;
In
tert-butyl alcohol;
Sealed tube;
Inert atmosphere;
With
hydrogen;
In
tert-butyl alcohol;
at 80 ℃;
for 18h;
under 22502.3 Torr;
Autoclave;
|
98 %Chromat.
|
|
Multi-step reaction
with
2
steps
1: C16
H11
BrMnN3
O3
/ tetrahydrofuran / 24 h / 120 °C / Inert atmosphere; Sealed tube
2: sodium hydroxide; water / tetrahydrofuran; methanol / 20 °C
With
water; C16H11BrMnN3O3; sodium hydroxide;
In
tetrahydrofuran; methanol;
|
2.What is the CAS number for 4-tert-Butylbenzylamine ?
The CAS number of 4-tert-Butylbenzylamine is 39895-55-1.
More information of 4-tert-Butylbenzylamine 39895-55-1 are:
|
CAS?Number |
39895-55-1 |
|
Density |
0.927 g/cm3 |
|
Boiling Point |
241.4 °C at 760 mmHg |
|
Flash Point |
104.8 °C |
|
Vapor Pressure |
0.036mmHg at 25°C |
|
Refractive Index |
1.52-1.522 |
|
HS CODE |
29214990 |
|
PSA |
26.02000 |
|
LogP |
3.14310 |
|
Pka |
9.24±0.10(Predicted) |
3.What are another words for 4-tert-Butylbenzylamine ?
Synonyms?for?4-tert-Butylbenzylamine 39895-55-1:(4-tert-Butylphenyl)methanamine;4-t-Butylbenzylamine;[(4-tert-Butylphenyl)methyl]amine;p-tert-Butylbenzylamine;
4.What is the molecular formula of 4-tert-Butylbenzylamine?
The chemical formula of ?4-tert-Butylbenzylamine is?C11H17N which containing 11 Carbon atoms,17 Hydrogen atoms and 1 Nitrogen atoms,and the molecular weight of??4-tert-Butylbenzylamine?is 163.263.
5.What is 4-tert-Butylbenzylamine (39895-55-1) used for?
4-tert-Butylbenzylamine is an organic compound characterized by the presence of a tert-butyl group attached to a benzene ring, with an amine functional group attached to the benzylic carbon. It is known for its reactivity and stability, making it a versatile building block in various chemical reactions.
InChI:InChI=1/C11H17N/c1-11(2,3)10-6-4-9(8-12)5-7-10/h4-7H,8,12H2,1-3H3
Relevant articles related to 4-tert-Butylbenzylamine:
|
Article |
Source |
|
Ultra-small cobalt nanoparticles from molecularly-defined Co-salen complexes for catalytic synthesis of amines |
Beller, Matthias,Chandrashekhar, Vishwas G.,Gawande, Manoj B.,Jagadeesh, Rajenahally V.,Kalevaru, Narayana V.,Kamer, Paul C. J.,Senthamarai, Thirusangumurugan,Zbo?il, Radek , p. 2973 - 2981 (2020/03/27) |
|
Reusable Nickel Nanoparticles-Catalyzed Reductive Amination for Selective Synthesis of Primary Amines |
Murugesan, Kathiravan,Beller, Matthias,Jagadeesh, Rajenahally V. supporting information, p. 5064 - 5068 (2019/03/19) |
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