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66636-17-7

Benzoic acid, 3,4-bis[[(1,1-dimethylethoxy)carbonyl]amino]-

Catalog#: AR00H8LE  |   CAS#: 66636-17-7  |   MDL#: MFCD02682245  |   MF: C17H24N2O6  |   MW: 352.38225999999986

Packsize Purity Price Availability Quantity
250mg 97% $41.00 Global Stock Buy Now Add To Cart
1g 97% $108.00 Global Stock Buy Now Add To Cart
5g 97% $391.00 Global Stock Buy Now Add To Cart
10g 97% $663.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00H8LE
Chemical Name Benzoic acid, 3,4-bis[[(1,1-dimethylethoxy)carbonyl]amino]-
CAS Number 66636-17-7
Molecular Formula C17H24N2O6
Molecular Weight 352.38225999999986
MDL Number MFCD02682245
SMILES O=C(OC(C)(C)C)Nc1cc(ccc1NC(=O)OC(C)(C)C)C(=O)O

Di-Boc-3,4-diaminobenzoic acid is a versatile chemical compound commonly used in chemical synthesis as a protective group reagent. In the realm of organic chemistry, it serves a crucial role in the protection of amine functionalities. By attaching a Di-Boc (di-tert-butoxycarbonyl) group to the amino group of the benzoic acid, it effectively shields the amine from unwanted reactions or interactions during various synthetic processes.This safeguarding property of Di-Boc-3,4-diaminobenzoic acid is particularly beneficial in multi-step organic syntheses where selective reactions are vital. The reversible nature of the Di-Boc protection allows chemists to manipulate the amine group as needed while preventing any undesired side reactions. Subsequently, this controlled reactivity enables the synthesis of complex molecules with precise functional group manipulations.Moreover, Di-Boc-3,4-diaminobenzoic acid's compatibility with a variety of reaction conditions and its ease of removal post-synthesis make it a valuable tool in organic synthesis. Its application extends to the creation of pharmaceuticals, agrochemicals, and other fine chemicals, where precise protection and deprotection steps are essential for successful compound production.
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