AB24842
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
10g | in stock | $8.00 | $5.00 | - + | ||
25g | in stock | $9.00 | $6.00 | - + | ||
100g | in stock | $13.00 | $9.00 | - + | ||
500g | in stock | $38.00 | $26.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB24842 |
Chemical Name: | 2,6-Diisopropylaniline |
CAS Number: | 24544-04-5 |
Molecular Formula: | C12H19N |
Molecular Weight: | 177.286 |
MDL Number: | MFCD00008887 |
SMILES: | CC(c1cccc(c1N)C(C)C)C |
Complexity: | 135 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 2 |
XLogP3: | 3.2 |
2,6-Diisopropylaniline is a versatile compound widely used in chemical synthesis processes. Its primary application lies in the field of organic chemistry, where it serves as a key building block in the synthesis of various organic compounds. Due to its unique structure and reactivity, 2,6-Diisopropylaniline is particularly valued for its ability to participate in a variety of reactions, including acylation, alkylation, and condensation reactions.In organic synthesis, 2,6-Diisopropylaniline can be utilized as a valuable intermediate in the production of dyes, pharmaceuticals, agrochemicals, and other fine chemicals. Its presence in a reaction mixture can facilitate the formation of complex molecular structures with specific functional groups and stereochemistry. Additionally, the steric hindrance provided by the diisopropyl groups in 2,6-Diisopropylaniline can influence the regioselectivity and stereoselectivity of certain reactions, leading to the production of desired products with high purity and yield.Furthermore, the unique electronic properties of 2,6-Diisopropylaniline make it a valuable reagent in the synthesis of various heterocyclic compounds, such as indoles, pyrroles, and benzimidazoles. Its ability to undergo diverse transformations under mild reaction conditions makes it a versatile tool for organic chemists seeking to develop new synthetic routes and expand the scope of their chemical toolbox.Overall, 2,6-Diisopropylaniline plays a crucial role in the realm of chemical synthesis, offering synthetic chemists a valuable building block for the construction of complex organic molecules with tailored properties and functionalities.
Dalton transactions (Cambridge, England : 2003) 20121107
Dalton transactions (Cambridge, England : 2003) 20120828
Dalton transactions (Cambridge, England : 2003) 20120714
Acta crystallographica. Section E, Structure reports online 20120301
Acta crystallographica. Section E, Structure reports online 20111201
Acta crystallographica. Section E, Structure reports online 20110901
Analytical and bioanalytical chemistry 20110601
Acta crystallographica. Section E, Structure reports online 20110601
Acta crystallographica. Section E, Structure reports online 20110501
Dalton transactions (Cambridge, England : 2003) 20110314
Acta crystallographica. Section E, Structure reports online 20110201
Acta crystallographica. Section E, Structure reports online 20091101
Dalton transactions (Cambridge, England : 2003) 20091007
Dalton transactions (Cambridge, England : 2003) 20090621
Acta crystallographica. Section E, Structure reports online 20090301
Dalton transactions (Cambridge, England : 2003) 20090107
Acta crystallographica. Section E, Structure reports online 20081201
Acta crystallographica. Section E, Structure reports online 20080901
Acta crystallographica. Section E, Structure reports online 20080801
The Journal of organic chemistry 20071012
Chemistry (Weinheim an der Bergstrasse, Germany) 20070101
Beilstein journal of organic chemistry 20070101
Journal of the American Chemical Society 20061220
Dalton transactions (Cambridge, England : 2003) 20060521
Inorganic chemistry 20051212
Journal of the American Chemical Society 20040526
Organic & biomolecular chemistry 20040221
Inorganic chemistry 20021216
Inorganic chemistry 20021118