1080-44-0 | N-P-Tosylglycine

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$14.00	$10.00
5g	97%	in stock	$16.00	$11.00
25g	97%	in stock	$32.00	$22.00
100g	97%	in stock	$112.00	$78.00

Description

• Catalog Number: AD78486
• Chemical Name: N-P-Tosylglycine
• CAS Number: 1080-44-0
• Molecular Formula: C9H11NO4S
• Molecular Weight: 229.25293999999997
• MDL Number: MFCD03092531
• SMILES: OC(=O)CNS(=O)(=O)c1ccc(cc1)C
• NSC Number: 25821

Computed Properties

• Complexity: 312
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4
• XLogP3: 0.8

Upstream Synthesis Route

The compound Glycine, N-[(4-methylphenyl)sulfonyl]- is a versatile intermediate commonly used in chemical synthesis. This unique compound serves as a key building block for the creation of various organic molecules and functional materials. Its sulfonamide moiety provides reactivity that enables the formation of complex molecular structures through different synthetic routes. Glycine, N-[(4-methylphenyl)sulfonyl]- plays a crucial role in the development of pharmaceuticals, agrochemicals, and advanced materials due to its ability to undergo selective chemical transformations. Its significance as a synthetic tool is highlighted by its wide applications in medicinal chemistry, material science, and pharmaceutical industry.

Literature

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• Aqua-{N-[(4-methyl-phen-yl)sulfon-yl]glycinato(2-)-κN,O}(1,10-phenan-throline)copper(II).

  Acta crystallographica. Section E, Structure reports online 20101001

• Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives.

  Beilstein journal of organic chemistry 20070101