120-07-0 | N-Phenyldiethanolamine

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$15.00	$10.00
5g	97%	in stock	$16.00	$11.00
25g	97%	in stock	$18.00	$12.00
100g	97%	in stock	$20.00	$14.00
500g	97%	in stock	$88.00	$62.00

Description

• Catalog Number: AB59446
• Chemical Name: N-Phenyldiethanolamine
• CAS Number: 120-07-0
• Molecular Formula: C10H15NO2
• Molecular Weight: 181.2316
• MDL Number: MFCD00002845
• SMILES: OCCN(c1ccccc1)CCO
• NSC Number: 6327

Computed Properties

• Complexity: 118
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 0.4

Upstream Synthesis Route

N-Phenyldiethanolamine is a versatile chemical compound commonly used in chemical synthesis as a multifunctional building block. This compound plays a crucial role in various organic reactions due to its unique structure and reactivity. In chemical synthesis, N-Phenyldiethanolamine can act as a nucleophile, participating in reactions such as nucleophilic substitution and addition reactions. Its amine and alcohol functional groups make it a valuable reagent for forming bonds with electrophilic compounds. Additionally, the phenyl group provides aromatic properties that can influence the reactivity and selectivity of the compound in certain reactions.Moreover, N-Phenyldiethanolamine can be utilized as a ligand in transition metal-catalyzed reactions, where its amine group can coordinate with metal centers to facilitate various transformations. This compound's ability to form coordination complexes with metals enables it to promote catalytic processes with high efficiency and selectivity.Overall, N-Phenyldiethanolamine serves as a crucial component in the toolbox of synthetic chemists, offering a wide range of applications in organic synthesis, catalysis, and materials science.

Literature

• Some heterocyclic azo dyes derived from thiazolyl derivatives; synthesis; substituent effects and solvatochromic studies.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20101201

• Synthesis, photophysical properties, and self-assembly behavior of amphiphilic polyfluorene: unique dual fluorescence and its application as a fluorescent probe for the mercury ion.

  The journal of physical chemistry. B 20101125

• Two-stage sensing property via a conjugated donor-acceptor-donor constitution: application to the visual detection of mercuric ion.

  The Journal of organic chemistry 20050722