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Home Deuterated Building Blocks 6310-21-0
6310-21-0,MFCD00000794
Catalog No.:AA003HUW

6310-21-0 | 2-tert-Butylaniline

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$14.00   $10.00
- +
5g
98%
in stock  
$17.00   $12.00
- +
10g
98%
in stock  
$22.00   $15.00
- +
25g
98%
in stock  
$44.00   $31.00
- +
100g
98%
in stock  
$173.00   $121.00
- +
500g
98%
in stock  
$857.00   $600.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003HUW
Chemical Name:
2-tert-Butylaniline
CAS Number:
6310-21-0
Molecular Formula:
C10H15N
Molecular Weight:
149.2328
MDL Number:
MFCD00000794
SMILES:
Nc1ccccc1C(C)(C)C
NSC Number:
43044
Properties
Properties
 
BP:
123-124°C at 760 mmHg  
Form:
Liquid  
MP:
149.23 °C  
Refractive Index:
n20/D 1.545(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
123  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
3  

Literature

Title: Bis(μ-2-tert-butyl-phenyl-imido-1:2κN:N)chlorido-2κCl-(diethyl ether-1κO)(2η-penta-methyl-cyclo-penta-dien-yl)lithiumtantalum(V).

Journal: Acta crystallographica. Section E, Structure reports online 20110601

Title: Regioselective copper-catalyzed amination of chlorobenzoic acids: synthesis and solid-state structures of N-aryl anthranilic acid derivatives.

Journal: The Journal of organic chemistry 20060106

Title: Synthesis of optically active atropisomeric anilide derivatives through diastereoselective N-allylation with a chiral Pd-pi-allyl catalyst.

Journal: The Journal of organic chemistry 20031212

Title: C-C bond formation via C-H bond activation: catalytic arylation and alkenylation of alkane segments.

Journal: Journal of the American Chemical Society 20021113

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SDS
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