57561-39-4 | Boc,Me-glycinol

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$5.00	$4.00
10g	98%	in stock	$6.00	$5.00
25g	98%	in stock	$13.00	$10.00
100g	98%	in stock	$51.00	$36.00
500g	98%	in stock	$254.00	$178.00
1000g	98%	in stock	$432.00	$303.00

Description

• Catalog Number: AB43502
• Chemical Name: Boc,Me-glycinol
• CAS Number: 57561-39-4
• Molecular Formula: C8H17NO3
• Molecular Weight: 175.2255
• MDL Number: MFCD03425857
• SMILES: OCCN(C(=O)OC(C)(C)C)C

Computed Properties

• Complexity: 151
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 4
• XLogP3: 0.4

Upstream Synthesis Route

N-Boc-N-methylethanolamine is a versatile compound that finds wide applications in chemical synthesis, particularly in the field of organic chemistry. It serves as a valuable building block in the synthesis of various complex organic molecules due to its unique structural properties and reactivity.This compound can be utilized as a protecting group for amines in organic synthesis. By selectively masking the amino group with the Boc (tert-butoxycarbonyl) protecting group, N-Boc-N-methylethanolamine allows for the manipulation of specific functional groups within a molecule without interfering with the amine functionality. This protection strategy enables chemists to control the reactivity and selectivity of reactions, leading to the efficient formation of desired compounds.Furthermore, N-Boc-N-methylethanolamine can serve as a precursor in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its presence in the chemical toolbox offers synthetic chemists the flexibility to access structurally diverse molecules through strategic deprotection and functional group transformations.In summary, the application of N-Boc-N-methylethanolamine in chemical synthesis provides a powerful tool for the design and construction of complex organic molecules with precision and efficiency. Its versatility and reactivity make it an indispensable reagent in the repertoire of synthetic chemists seeking to access diverse chemical space.