60022-62-0 | L-Serine benzyl ester, HCl

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$13.00	$9.00
5g	95%	in stock	$16.00	$11.00
10g	95%	in stock	$20.00	$14.00
25g	95%	in stock	$24.00	$17.00
100g	95%	in stock	$95.00	$67.00
500g	95%	in stock	$474.00	$332.00

Description

• Catalog Number: AB46255
• Chemical Name: L-Serine benzyl ester, HCl
• CAS Number: 60022-62-0
• Molecular Formula: C10H14ClNO3
• Molecular Weight: 231.6761
• MDL Number: MFCD00038955
• SMILES: OC[C@@H](C(=O)OCc1ccccc1)N.Cl

Computed Properties

• Complexity: 178
• Covalently-Bonded Unit Count: 2
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 5

Upstream Synthesis Route

H-Ser-Obzl Hcl, also known as N-t-butoxycarbonyl-Serine benzylester hydrochloride, is a key reagent commonly used in chemical synthesis processes. This compound is particularly valued for its significant role in peptide synthesis, where it serves as a crucial building block for creating complex peptides.In chemical synthesis, H-Ser-Obzl Hcl acts as a protected form of serine, an amino acid essential for the construction of peptides and proteins. By incorporating this reagent into a synthesis reaction, chemists can selectively introduce serine at specific positions within a peptide chain without undesired side reactions. This level of control is essential for the precise assembly of peptides with specific sequences and functions.Furthermore, H-Ser-Obzl Hcl allows chemists to manipulate peptide structures with high efficiency and accuracy. Its use in peptide synthesis enables the creation of customized peptides for various applications, such as pharmaceuticals, bioengineering, and biochemical research. The protection provided by this reagent helps ensure the stability of the serine component during synthesis, leading to improved yields and purity of the final peptide product.Overall, the application of H-Ser-Obzl Hcl in chemical synthesis plays a critical role in expanding the capabilities of peptide chemistry and facilitating the development of novel peptide-based materials and therapeutics.