88568-95-0 | (+/-)-Benzyloxycarbonyl-alpha-phosphonoglycine trimethyl ester

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$8.00	$5.00
10g	98%	in stock	$10.00	$7.00
25g	98%	in stock	$18.00	$12.00
50g	98%	in stock	$33.00	$23.00
100g	98%	in stock	$65.00	$45.00

Description

• Catalog Number: AB47298
• Chemical Name: (+/-)-Benzyloxycarbonyl-alpha-phosphonoglycine trimethyl ester
• CAS Number: 88568-95-0
• Molecular Formula: C13H18NO7P
• Molecular Weight: 331.2583
• MDL Number: MFCD00043304
• SMILES: COC(=O)C(P(=O)(OC)OC)NC(=O)OCc1ccccc1

Computed Properties

• Complexity: 415
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 22
• Hydrogen Bond Acceptor Count: 7
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 9
• Undefined Atom Stereocenter Count: 1
• XLogP3: 0.7

Upstream Synthesis Route

Methyl N-(benzyloxycarbonyl)-2-(dimethylphosphono)glycinate, also known as $name$, is a valuable compound widely used in chemical synthesis for its unique properties and versatile applications. This compound serves as a key building block in the synthesis of various complex organic molecules, particularly in the field of pharmaceuticals and agrochemicals.One of the primary applications of $name$ in chemical synthesis is its role as a protecting group for the amino group in amino acids and peptides. By selectively masking the amino group with the benzyloxycarbonyl (Cbz) protecting group, $name$ allows for specific reactions to occur at other functional groups within the molecule without affecting the amino group. This helps in controlling the reactivity and selectivity of the reactions, leading to efficient synthesis of peptide-based drugs and bioactive compounds.Moreover, the dimethylphosphono group in $name$ provides an additional functionality that can be further utilized in various synthetic transformations. The phosphono group can act as a directing group in organometallic chemistry, enabling selective C-C bond formations and other valuable reactions. This enhances the synthetic versatility of $name$ and opens up opportunities for the construction of structurally diverse and complex molecules.Overall, the strategic incorporation of Methyl N-(benzyloxycarbonyl)-2-(dimethylphosphono)glycinate in chemical synthesis enables chemists to carry out precise and efficient reactions, ultimately facilitating the synthesis of biologically active compounds and novel materials.