2-[(1-Naphthyloxy)methyl]oxirane

• CAS: 2461-42-9
• Catalog Number: ACM2461429
• Category: Main Products
• Molecular Weight: 200.23
• Molecular Formula: C₁₃H₁₂O₂
• Synonyms: NAPHTHYL GLYCIDYL ETHER;1-(2,3-epoxypropoxy)-naphthalen;1-naphthylglycidylether;ether,2,3-epoxypropyl1-naphthyl;glycidyl1-naphthylether;1-(ALPHA-NAPHTHALENOXY)-2,3-EPOXYPROPANE;1-NAPHTHOL GLYCIDYL ETHER;2-[(1-NAPHTHYLOXY)METHYL]OXIRANE
• IUPAC Name: α-Naphthyl Glycidyl Ether
• Boiling Point: 163-167
• Flash Point: 152ºC
• Density: 1.192 g/cm³
• Appearance: Light purple oil
• Exact Mass: 200.08400

Custom Q&A

What is the molecular formula of the compound?

The molecular formula of the compound is C13H12O2.

What are the synonyms of the compound?

The synonyms of the compound are:
Glycidyl 1-naphthyl ether
2-[(1-Naphthyloxy)methyl]oxirane
2-((Naphthalen-1-yloxy)methyl)oxirane
Naphthyl glycidyl ether

What is the molecular weight of the compound?

The molecular weight of the compound is 200.23 g/mol.

When was the compound created and last modified?

The compound was created on March 26, 2005, and last modified on October 21, 2023.

What is the IUPAC name of the compound?

The IUPAC name of the compound is 2-(naphthalen-1-yloxymethyl)oxirane.

What is the InChI of the compound?

The InChI of the compound is: InChI=1S/C13H12O2/c1-2-6-12-10(4-1)5-3-7-13(12)15-9-11-8-14-11/h1-7,11H,8-9H2.

What is the InChIKey of the compound?

The InChIKey of the compound is: QYYCPWLLBSSFBW-UHFFFAOYSA-N.

What is the canonical SMILES of the compound?

The canonical SMILES of the compound is: C1C(O1)COC2=CC=CC3=CC=CC=C32.

What is the CAS number of the compound?

The CAS number of the compound is 2461-42-9.

What is the XLogP3 value of the compound?

The XLogP3 value of the compound is 3.3.

Synthetic Use

Upstream Synthesis Route 1

• 90-15-3
• 106-89-8

• 2461-42-9

Reference: [1]Location in patent: experimental part
Narsaiah, A. Venkat; Wadavrao, Sachin B.; Reddy, A. Ramesh; Yadav
[Synthesis, 2011, # 3, p. 485 - 489]
[2]Pollard; Ingwalson
[Journal of the American Chemical Society, 1955, vol. 77, p. 3402]

Downstream Synthesis Route 1

• 2461-42-9
• 35386-24-4

• 57149-07-2

Reference: [1] Patent: US2015/353473, 2015, A1, . Location in patent: Paragraph 0179-0181

Downstream Synthesis Route 2

• 2461-42-9
• 75-31-0

• 318-98-9

Reference: [1] Chemical and Pharmaceutical Bulletin, 1981, vol. 29, # 8, p. 2246 - 2250

Downstream Synthesis Route 3

• 2461-42-9
• 10576-12-2

• 67435-09-0

Reference: [1]Patent: DE2651083,1978,

* For details of the synthesis route, please refer to the original source to ensure accuracy.