116026-98-3 | tert-Butyl 2-bromopyridin-3-ylcarbamate

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$29.00	$21.00
1g	98%	in stock	$76.00	$54.00
5g	98%	in stock	$372.00	$261.00
10g	98%	in stock	$744.00	$521.00
25g	98%	in stock	$1,664.00	$1,165.00

Description

• Catalog Number: AA14612
• Chemical Name: tert-Butyl 2-bromopyridin-3-ylcarbamate
• CAS Number: 116026-98-3
• Molecular Formula: C10H13BrN2O2
• Molecular Weight: 273.1264
• MDL Number: MFCD07367911
• SMILES: O=C(Nc1cccnc1Br)OC(C)(C)C

Computed Properties

• Complexity: 228
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 2.4

Upstream Synthesis Route

Tert-Butyl (2-bromopyridin-3-yl)carbamate is a valuable compound widely used in chemical synthesis. Its application in organic chemistry primarily lies in its functional group reactivity and versatility. This compound serves as a useful building block for the synthesis of various organic molecules and pharmaceutical intermediates.One of the key applications of tert-Butyl (2-bromopyridin-3-yl)carbamate is in the preparation of heterocyclic compounds. By utilizing its bromopyridine moiety, chemists can introduce diversity into molecular structures, enabling the creation of complex molecules with specific functionalities. The tert-butyl carbamate group can also serve as a protecting group, allowing selective modification of other reactive sites in a molecule without affecting the desired functional group.Furthermore, this compound can participate in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce additional substituents or building blocks onto the pyridine ring. The ease of functional group manipulation in tert-Butyl (2-bromopyridin-3-yl)carbamate makes it a valuable tool for designing and synthesizing novel organic compounds with tailored properties.In summary, tert-Butyl (2-bromopyridin-3-yl)carbamate is a versatile intermediate that plays a crucial role in the construction of complex organic molecules, making it indispensable in modern chemical synthesis strategies.