2,7-Dibromonaphthalene

• CAS: 58556-75-5
• Catalog Number: ACM58556755
• Category: Aryl
• Molecular Weight: 285.96g/mol
• Molecular Formula: C10H6Br2
• IUPAC Name: 2,7-dibromonaphthalene
• Canonical SMILES: C1=CC(=CC2=C1C=CC(=C2)Br)Br
• InChI: InChI=1S/C10H6Br2/c11-9-3-1-7-2-4-10(12)6-8(7)5-9/h1-6H
• InChI Key: ODJZWBLNJKNOJK-UHFFFAOYSA-N
• Complexity: 142
• Covalently-Bonded Unit Count: 1
• Exact Mass: 285.88158g/mol
• Formal Charge: 0
• Hazard Statements: H315-H319-H335
• H-Bond Acceptor: 0
• H-Bond Donor: 0
• Heavy Atom Count: 12
• Monoisotopic Mass: 283.88363g/mol
• RIDADR: NONH for all modes of transport
• Rotatable Bond Count: 0
• Symbol: GHS07
• XLogP3: 4.6

Custom Q&A

What is the molecular formula of 2,7-Dibromonaphthalene?

The molecular formula of 2,7-Dibromonaphthalene is C10H6Br2.

When was 2,7-Dibromonaphthalene first created according to the reference?

2,7-Dibromonaphthalene was first created on March 28, 2005.

What is the IUPAC name of 2,7-Dibromonaphthalene?

The IUPAC name of 2,7-Dibromonaphthalene is 2,7-dibromonaphthalene.

What is the InChIKey of 2,7-Dibromonaphthalene?

The InChIKey of 2,7-Dibromonaphthalene is ODJZWBLNJKNOJK-UHFFFAOYSA-N.

What is the canonical SMILES of 2,7-Dibromonaphthalene?

The canonical SMILES of 2,7-Dibromonaphthalene is C1=CC(=CC2=C1C=CC(=C2)Br)Br.

What is the molecular weight of 2,7-Dibromonaphthalene?

The molecular weight of 2,7-Dibromonaphthalene is 285.96 g/mol.

What is the CAS number for 2,7-Dibromonaphthalene?

The CAS number for 2,7-Dibromonaphthalene is 58556-75-5.

What is the XLogP3-AA value for 2,7-Dibromonaphthalene?

The XLogP3-AA value for 2,7-Dibromonaphthalene is 4.6.

How many hydrogen bond donor counts does 2,7-Dibromonaphthalene have?

2,7-Dibromonaphthalene has 0 hydrogen bond donor counts.

Is 2,7-Dibromonaphthalene a covalently-bonded unit according to the reference?

Yes, 2,7-Dibromonaphthalene is a covalently-bonded unit.

Synthetic Use

Upstream Synthesis Route 1

• 582-17-2

• 58556-75-5

Reference: [1] Arkivoc, 2011, vol. 2011, # 6, p. 176 - 198

Upstream Synthesis Route 2

• 92-41-1

• 58556-75-5

Reference: [1] Journal of the Indian Chemical Society, 1939, vol. 16, p. 460
[2] Bulletin de la Societe Chimique de France, 1877, vol. <2> 28, p. 516

Upstream Synthesis Route 3

• 861339-85-7

• 58556-75-5

Reference: [1] Journal fuer Praktische Chemie (Leipzig), 1921, vol. <2> 101, p. 61

Upstream Synthesis Route 4

• 92-41-1

• 58556-75-5

Reference: [1]Journal of the Indian Chemical Society,1939,vol. 16,p. 460
[2]Bulletin de la Societe Chimique de France,1877,vol. <2> 28,p. 516

Upstream Synthesis Route 5

• 861339-85-7

• 58556-75-5

Reference: [1]Journal fur praktische Chemie (Leipzig 1954),1921,vol. <2> 101,p. 61

Upstream Synthesis Route 6

• 582-17-2

• 58556-75-5

Reference: [1]ARKIVOC,2011,vol. 2011,p. 176 - 198
[2]Angewandte Chemie - International Edition,2018,vol. 57,p. 12102 - 12105
Angew. Chem.,2018,vol. 130,p. 12278 - 12281,4
[3]Journal of the American Chemical Society,1982,vol. 104,p. 346 - 347
[4]Journal of Organometallic Chemistry,1977,vol. 128,p. 95 - 98
[5]Journal of Organic Chemistry,1988,vol. 53,p. 2489 - 2496