7-Methoxy-2-tetralone

• CAS: 4133-34-0
• Catalog Number: ACM4133340
• Category: Other Products
• Molecular Weight: 176.21
• Molecular Formula: C₁₁H₁₂O₂
• Synonyms: 7-METHOXY-3,4-DIHYDRONAPHTHALEN-2(1H)-ONE;7-METHOXY-2-TETRALONE;3,4-DIHYDRO-7-METHOXY-2(1H)-NAPHTHALENONE;2(1H)-NAPHTHALENONE, 3,4-DIHYDRO-7-METHOXY-;7-methoxy-1,2,3,4-tetrahydronaphthalen-2-one;7-Methoxy-2-Tetralone(7-OHO);7-Methoxyl-2-Tetralone;7-Methoxy-3,4-dihydronaphthalen-2(1H)-one 97%
• Boiling Point: 124-126°C1.5mm Hg(lit.)
• Flash Point: >230°F
• Density: 1.13g/mL at 25°C(lit.)
• Hazard Statements: Xi,Xn
• Safety Description: 24/25-36-26

Custom Q&A

What is the molecular formula of 7-Methoxy-2-tetralone?

The molecular formula of 7-Methoxy-2-tetralone is C11H12O2.

What is the molecular weight of 7-Methoxy-2-tetralone?

The molecular weight of 7-Methoxy-2-tetralone is 176.21 g/mol.

What is the IUPAC name of 7-Methoxy-2-tetralone?

The IUPAC name of 7-Methoxy-2-tetralone is 7-methoxy-3,4-dihydro-1H-naphthalen-2-one.

What is the InChI of 7-Methoxy-2-tetralone?

The InChI of 7-Methoxy-2-tetralone is InChI=1S/C11H12O2/c1-13-11-5-3-8-2-4-10(12)6-9(8)7-11/h3,5,7H,2,4,6H2,1H3.

What is the InChIKey of 7-Methoxy-2-tetralone?

The InChIKey of 7-Methoxy-2-tetralone is XEAPZXNZOJGVCZ-UHFFFAOYSA-N.

What is the canonical SMILES of 7-Methoxy-2-tetralone?

The canonical SMILES of 7-Methoxy-2-tetralone is COC1=CC2=C(CCC(=O)C2)C=C1.

What is the CAS number of 7-Methoxy-2-tetralone?

The CAS number of 7-Methoxy-2-tetralone is 4133-34-0.

What is the European Community (EC) number of 7-Methoxy-2-tetralone?

The European Community (EC) number of 7-Methoxy-2-tetralone is 223-954-1.

What is the UNII of 7-Methoxy-2-tetralone?

The UNII of 7-Methoxy-2-tetralone is WF978B639S.

Is 7-Methoxy-2-tetralone a canonicalized compound?

Yes, 7-Methoxy-2-tetralone is a canonicalized compound.

Synthetic Use

Upstream Synthesis Route 1

• 1048330-08-0

• 4133-34-0

Reference: [1] Journal of Medicinal Chemistry, 2008, vol. 51, # 15, p. 4804 - 4822

Upstream Synthesis Route 2

• 1190847-93-8

• 4133-34-0

Reference: [1] Tetrahedron Letters, 2009, vol. 50, # 41, p. 5713 - 5715

Upstream Synthesis Route 3

• 63320-02-5

• 4133-34-0

Reference: [1] Journal of Medicinal Chemistry, 1998, vol. 41, # 21, p. 4036 - 4052
[2] Journal of Medicinal Chemistry, 1989, vol. 32, # 5, p. 961 - 968

Downstream Synthesis Route 1

• 4133-34-0
• 5052-95-9

• 38205-25-3

Reference: [1]Journal of medicinal chemistry,1972,vol. 15,p. 1123 - 1128

Downstream Synthesis Route 2

• 4133-34-0
• 74-88-4

• 1865-83-4

Reference: [1]Location in patent: experimental part
Liese, Julia; Hampp, Norbert A.
[Journal of Photochemistry and Photobiology A: Chemistry, 2010, vol. 209, # 2-3, p. 128 - 134]

Downstream Synthesis Route 3

• 4133-34-0

• 4003-89-8

Reference: [1]Journal of Enzyme Inhibition and Medicinal Chemistry,2015,vol. 30,p. 406 - 412

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