2-Iodonaphthalene

• CAS: 612-55-5
• Catalog Number: ACM612555
• Category: Aryl
• Molecular Weight: 254.07
• Molecular Formula: C₁₀H₆Br₂
• Synonyms: 2-Iodonaphthalene, Naphthalene, 2-iodo-, 2-iodo-naphtalene, 2-Naphthyl iodide, beta-Iodonaphthalene, .beta.-Iodonaphthalene, NSC3786, CID136412, BBV-2091927, AC-907/25004996, S14-0867, 612-55-5, InChI=1/C10H7I/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7
• IUPAC Name: 2-iodonaphthalene
• SMILES: C1=CC=C2C=C(C=CC2=C1)I
• InChI Key: FRNLBIWVMVNNAZ-UHFFFAOYSA-N
• Boiling Point: 307.5ºC at 760 mmHg
• Melting Point: 52-56ºC
• Flash Point: 138.4ºC
• Density: 1.744 g/cm³
• Exact Mass: 253.95900
• Hazard Statements: H302-H410
• H-Bond Acceptor: 0
• H-Bond Donor: 0
• RIDADR: NONH for all modes of transport
• Symbol: GHS07

Custom Q&A

What is the molecular formula of 2-Iodonaphthalene?

The molecular formula of 2-Iodonaphthalene is C10H7I.

What is the molecular weight of 2-Iodonaphthalene?

The molecular weight of 2-Iodonaphthalene is 254.07 g/mol.

What is the IUPAC name of 2-Iodonaphthalene?

The IUPAC name of 2-Iodonaphthalene is 2-iodonaphthalene.

What is the InChI of 2-Iodonaphthalene?

The InChI of 2-Iodonaphthalene is InChI=1S/C10H7I/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H.

What is the InChIKey of 2-Iodonaphthalene?

The InChIKey of 2-Iodonaphthalene is FRNLBIWVMVNNAZ-UHFFFAOYSA-N.

What is the canonical SMILES of 2-Iodonaphthalene?

The canonical SMILES of 2-Iodonaphthalene is C1=CC=C2C=C(C=CC2=C1)I.

What is the CAS number of 2-Iodonaphthalene?

The CAS number of 2-Iodonaphthalene is 612-55-5.

What is the European Community (EC) number of 2-Iodonaphthalene?

The European Community (EC) number of 2-Iodonaphthalene is 627-170-4.

What is the DSSTox Substance ID of 2-Iodonaphthalene?

The DSSTox Substance ID of 2-Iodonaphthalene is DTXSID00210107.

Is 2-Iodonaphthalene a canonicalized compound?

Yes, 2-Iodonaphthalene is a canonicalized compound according to PubChem.

Synthetic Use

Upstream Synthesis Route 1

• 91-20-3

• 612-55-5
• 90-14-2

Reference: [1] Russian Journal of Organic Chemistry, 2005, vol. 41, # 6, p. 855 - 859
[2] Journal of Organic Chemistry, 2018, vol. 83, # 2, p. 930 - 938

Upstream Synthesis Route 2

• 91-20-3

• 612-55-5
• 90-14-2
• 36316-88-8

Reference: [1] Journal of Catalysis, 1994, vol. 147, # 1, p. 186 - 198
[2] Journal of Catalysis, 1994, vol. 147, # 1, p. 186 - 198

Upstream Synthesis Route 3

• 580-13-2

• 612-55-5

Reference: [1]Organometallics,2011,vol. 30,p. 4067 - 4073

Downstream Synthesis Route 1

• 1592-95-6
• 612-55-5

• 934545-80-9

Reference: [1] Patent: US2017/162796, 2017, A1, . Location in patent: Paragraph 0134; 0135

Downstream Synthesis Route 2

• 141-32-2
• 612-55-5

• 124182-61-2

Reference: [1]Tetrahedron Letters,2020,vol. 61
[2]Chemistry of Heterocyclic Compounds,1983,p. 156 - 160
Khimiya Geterotsiklicheskikh Soedinenii,1983,vol. 19,p. 192 - 196

Downstream Synthesis Route 3

• 201230-82-2
• 612-55-5

• 93-09-4

Reference: [1]Synlett,2019,vol. 30,p. 961 - 966
[2]Journal of Organometallic Chemistry,1988,vol. 358,p. 563 - 566
[3]Beilstein Journal of Organic Chemistry,2016,vol. 12,p. 1503 - 1511
[4]ChemCatChem,2018,vol. 10,p. 1089 - 1095

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