107045-28-3 | tert-Butyl 4-(aminomethyl)benzoate

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$33.00	$24.00
250mg	95%	in stock	$42.00	$30.00
500mg	95%	in stock	$78.00	$55.00
1g	95%	in stock	$82.00	$58.00
5g	95%	in stock	$368.00	$258.00
25g	95%	in stock	$1,504.00	$1,053.00
100g	95%	in stock	$3,867.00	$2,707.00

Description

• Catalog Number: AD76591
• Chemical Name: tert-Butyl 4-(aminomethyl)benzoate
• CAS Number: 107045-28-3
• Molecular Formula: C12H17NO2
• Molecular Weight: 207.2689
• MDL Number: MFCD04973451
• SMILES: NCc1ccc(cc1)C(=O)OC(C)(C)C

Upstream Synthesis Route

In chemical synthesis, tert-Butyl 4-(aminomethyl)benzoate, also known as $name$, serves as a versatile building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound's unique molecular structure and reactivity make it a valuable tool in organic chemistry.One of the key applications of $name$ in chemical synthesis is as a precursor for the synthesis of complex organic molecules. By utilizing the reactive amine group and the tert-butyl ester functionality, chemists can introduce this moiety into target molecules, enabling the construction of intricate chemical structures with high efficiency and selectivity.Moreover, the presence of the tert-butyl group in $name$ provides steric hindrance, which can influence the regioselectivity and stereochemistry of subsequent reactions. This can be particularly advantageous in the synthesis of chiral compounds or in reactions where controlling the spatial orientation of functional groups is critical.Additionally, tert-Butyl 4-(aminomethyl)benzoate can also serve as a protecting group for amines during multi-step synthesis. By temporarily masking the amino group with the tert-butyl ester, chemists can prevent undesired reactions at this site and selectively deprotect it under controlled conditions when needed, facilitating the synthesis of complex molecules with multiple functional groups.Overall, the strategic use of tert-Butyl 4-(aminomethyl)benzoate in chemical synthesis enables chemists to access diverse chemical space, streamline synthetic routes, and overcome synthetic challenges, making it a valuable asset in the toolbox of organic chemists.