2-Naphthyl lactate

Base Information

• Chemical Name: 2-Naphthyl lactate
• CAS No.: 93-43-6
• Molecular Formula: C₁₃H₁₂O₃
• Molecular Weight: 216.236
• European Community (EC) Number: 202-246-6
• UNII: 8107M40WRT
• DSSTox Substance ID: DTXSID10883280
• Nikkaji Number: J182.094J
• Wikidata: Q27269182
• Mol file: 93-43-6.mol

Synonyms:lactonaphthol;2-Naphthyl lactate;93-43-6;lactol;(2-Methyloxiranyl)methanol;Propanoic acid, 2-hydroxy-, 2-naphthalenyl ester;UNII-8107M40WRT;8107M40WRT;EINECS 202-246-6;2-Hydroxypropanoic acid 2-naphthalenyl ester;2-naphthyllactat;naphthalen-2-yl 2-hydroxypropanoate;2-NAPHTHOL LACTATE;SCHEMBL18256;lactic acid beta-naphthyl ester;.BETA.-NAPHTHYL LACTATE;2-NAPHTHYL LACTATE [MI];DTXSID10883280;LACTIC ACID .BETA.-NAPHTHYL ESTER;Q27269182

Chemical Property of 2-Naphthyl lactate

Chemical Property:

• Vapor Pressure: 1.43E-06mmHg at 25°C
• Melting Point: 110-111 °C
• Boiling Point: 383.7°C at 760 mmHg
• Flash Point: 167.3°C
• PSA: 46.53000
• Density: 1.231g/cm³
• LogP: 2.12600
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 216.078644241
• Heavy Atom Count: 16
• Complexity: 252

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C(=O)OC1=CC2=CC=CC=C2C=C1)O

Technology Process of 2-Naphthyl lactate

There total 1 articles about 2-Naphthyl lactate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 86.0%

→ trans lactol (93-43-6)

Guidance literature:

Refernces

5-Acyloxy-5-hydroxymethyltetrahydro-2-furancarboxylate as a novel template for protein kinase C (PKC) binding

10.1016/S0014-827X(01)01077-1

The research focused on the development of a novel template, 5-acyloxy-5-hydroxymethyltetrahydro-2-furancarboxylate, for protein kinase C (PKC) binding. The purpose of this study was to synthesize and test a series of alkyl tetrahydrofuran-2-carboxylates as PKC ligands, which could potentially play a role in cellular signal transduction pathways and disease states. The researchers aimed to investigate whether these compounds could mimic a pharmacophore model comprising the C20–OH, C3–CO, and C9–OH groups, rather than the C13–CO moiety. The synthesis involved chemicals such as glycidyl 4-methoxyphenyl ether, lactol, 2-cyanotetrahydrofuran, and various esters, with the final compounds being 1–4. The study concluded that the new template did not offer significant advantages over previous models, and that finding a single isopharmacophoric group equivalent to phorbol’s C13–CO ester on simple conformationally constrained glycerol templates remains a challenge. The compounds showed binding affinities in the submicromolar range, similar to previous templates, indicating that the new template IV was not more effective than template I or II/III in terms of PKC binding affinity.

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