Catalog No.:AA0033AB

2142-70-3 | 2'-Iodoacetophenone

Name: Name:2'-Iodoacetophenone
Brand: AABLOCKS
SKU: AA0033AB
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
Request for Quotation
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA0033AB

Chemical Name:

2'-Iodoacetophenone

CAS Number:

2142-70-3

Molecular Formula:

C8H7IO

Molecular Weight:

246.0451

MDL Number:

MFCD00094998

SMILES:

CC(=O)c1ccccc1I

NSC Number:

46625

Properties

BP:

268.2°C at 760 mmHg

Form:

Liquid

Refractive Index:

n20/D 1.618(lit.)

Stability:

Light Sensitive

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

133

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

XLogP3:

2.3

Upstream Synthesis Route

2142-70-3

17408-14-9

[1]RSCAdvances,2016,vol.6,#55,p.50250-50254

2142-70-3

17408-14-9

[1]Chemistry--AEuropeanJournal,2015,vol.21,#1,p.96-100

122752-70-9

2142-70-3

[1]Tetrahedron,2014,vol.70,#52,p.9791-9796

[2]JournaloftheAmericanChemicalSociety,1996,vol.118,#25,p.5904-5918

[3]JournalofOrganicChemistry,2017,vol.82,#1,p.372-381

551-93-9

2142-70-3

[1]OrganicLetters,2015,vol.17,#21,p.5448-5451

[2]OrganicLetters,2015,vol.17,#24,p.6006-6009

[3]Synthesis,2007,#1,p.81-84

[4]Synthesis,2009,#6,p.941-944

[5]RussianJournalofOrganicChemistry,2008,vol.44,#8,p.1243-1244

[6]AdvancedSynthesisandCatalysis,2014,vol.356,#1,p.153-159

[7]ChemischeBerichte,1925,vol.58,p.48

615-42-9

108-24-7

2142-70-3

[1]Synthesis,2009,#16,p.2818-2824

Downstream Synthesis Route

2142-70-3

24017-95-6

[1]TetrahedronLetters,2014,vol.55,p.690-693

[2]Tetrahedron,2016,vol.72,p.5994-6000

[3]BulletinoftheChemicalSocietyofJapan,1980,vol.53,p.3691-3695

[4]RSCAdvances,2015,vol.5,p.74180-74188

[5]JournaloftheChemicalSociety,1958,p.1375,1378

[6]OrganicandBiomolecularChemistry,2009,vol.7,p.4853-4857

551-93-9

2142-70-3

[1]OrganicLetters,2015,vol.17,p.5448-5451

[2]OrganicLetters,2015,vol.17,p.6006-6009

[3]Synthesis,2007,p.81-84

[4]Synthesis,2009,p.941-944

[5]RussianJournalofOrganicChemistry,2008,vol.44,p.1243-1244

[6]AdvancedSynthesisandCatalysis,2014,vol.356,p.153-159

[7]ChemischeBerichte,1925,vol.58,p.48

[8]JournalofOrganicChemistry,2019,vol.84,p.9282-9296

[9]OrganicLetters,2019,vol.21,p.6648-6652

[10]AdvancedSynthesisandCatalysis,2019,vol.361,p.4581-4595

[11]JournalofOrganicChemistry,2020,vol.85,p.2438-2455

[12]OrganicLetters,2020

2142-70-3

20914-06-1

[1]BioorganicandMedicinalChemistryLetters,2018,vol.28,p.3441-3445

[2]JournalofPharmaceuticalSciences,1968,vol.57,p.1657-1661

35708-19-1

2142-70-3

99233-97-3

[1]ChemischeBerichte,1986,vol.119,p.3165-3197

2142-70-3

113258-84-7

[1]Patent:EP1215208,2002,A2.Locationinpatent:ExampleC(12)

[2]Patent:WO2016/131380,2016,A1.Locationinpatent:Paragraph281;282;283;284

[3]Patent:WO2017/75341,2017,A1.Locationinpatent:Paragraph00250;00251

[4]AngewandteChemie-InternationalEdition,2013,vol.52,p.7509-7513 Angew.Chem.,2013,vol.125,p.7657-7661,5

[5]JournaloftheChemicalSociety,1965,p.5537-5541

[6]OrganicLetters,2014,vol.16,p.302-305

[7]Patent:WO2016/132134,2016,A1.Locationinpatent:Page/Pagecolumn77;78

[8]JournalofMedicinalChemistry,2017,vol.60,p.1591-1597

Literature

Title: Trapping evidence for the thermal cyclization of di-(o-acetylphenyl)acetylene to 3,3'-dimethyl-1,1'-biisobenzofuran.

Journal: Beilstein journal of organic chemistry 20050101

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