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2243-82-5,MFCD00016812
Catalog No.:AA00BC7J

2243-82-5 | 2-Naphthylamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$19.00   $14.00
- +
5g
98%
in stock  
$28.00   $20.00
- +
10g
98%
in stock  
$55.00   $39.00
- +
25g
98%
in stock  
$136.00   $96.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00BC7J
Chemical Name:
2-Naphthylamide
CAS Number:
2243-82-5
Molecular Formula:
C11H9NO
Molecular Weight:
171.1953
MDL Number:
MFCD00016812
SMILES:
NC(=O)c1ccc2c(c1)cccc2
NSC Number:
171209
Properties
Computed Properties
 
Complexity:
202  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.6  

Downstream Synthesis Route

[1]Patent:WO2010/136755,2010,A1.Locationinpatent:Page/Pagecolumn65;66

[2]JournalofMedicinalChemistry,2006,vol.49,p.684-692

[3]Patent:US2007/105907,2007,A1.Locationinpatent:Page/PagecolumnSheet3/7;10

[4]JournaloftheAmericanChemicalSociety,1959,vol.81,p.3725,3726

[5]Patent:WO2004/108731,2004,A1.Locationinpatent:Page69

[1]ArchivderPharmazie,1927,vol.265,p.411

[1]ZhurnalObshcheiKhimii,1958,vol.28,p.1887,1889;engl.Ausg.S.1930,1932

[1]AngewandteChemie-InternationalEdition,2008,vol.47,p.3607-3609

[2]Synthesis,1980,p.243-244

[3]ChemistryLetters,2012,vol.41,p.633-635

[4]ChemicalCommunications,2009,p.3258-3260

[5]AppliedOrganometallicChemistry,2014,vol.28,p.900-907

[6]Catalysisscienceandtechnology,2015,vol.5,p.1606-1622

[7]TetrahedronLetters,2012,vol.53,p.2860-2863

[8]Chemistry-AEuropeanJournal,2017,vol.23,p.7761-7771

[9]CatalysisLetters,2018,vol.148,p.3378-3388

[10]EuropeanJournalofOrganicChemistry,2017,vol.2017,p.1870-1875

[11]NewJournalofChemistry,2018,vol.42,p.15221-15230

[12]Organometallics,2012,vol.31,p.3790-3797

[13]GreenChemistry,2014,vol.16,p.2136-2141

[14]GazzettaChimicaItaliana,1884,vol.14,p.122

[15]JournaloftheAmericanChemicalSociety,1917,vol.39,p.105

[16]JustusLiebigsAnnalenderChemie,1876,vol.180,p.305    ChemischeBerichte,1875,vol.8,p.1278

[17]AngewandteChemie-InternationalEdition,2012,vol.51,p.544-547

[18]ChemistryLetters,2012,vol.41,p.574-576

[19]SyntheticCommunications,2013,vol.43,p.2867-2875

[20]JournalofMolecularCatalysisA:Chemical,2015,vol.398,p.312-324

[21]Catalysisscienceandtechnology,2015,vol.5,p.3822-3828

[22]InorganicaChimicaActa,2016,vol.442,p.134-144

[1]AnnalesdeChimie(Cachan,France),1909,vol.<8>17,p.136

Literature

Title: Involvement of efflux mechanisms in biocide resistance of Campylobacter jejuni and Campylobacter coli.

Journal: Journal of medical microbiology 20120601

Title: Neoadjuvant chemotherapy modifies serum angiotensinase activities in women with breast cancer.

Journal: Maturitas 20120501

Title: Biochemical characterisation of prolyl aminopeptidase from shoots of triticale seedlings and its activity changes in response to suboptimal growth conditions.

Journal: Plant physiology and biochemistry : PPB 20111101

Title: Essential oils from Moroccan plants as potential chemosensitisers restoring antibiotic activity in resistant Gram-negative bacteria.

Journal: International journal of antimicrobial agents 20111001

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction.

Journal: Journal of combinatorial chemistry 20090112

Title: Synthesis and in vitro binding studies of substituted piperidine naphthamides. Part II: Influence of the substitution on the benzyl moiety on the affinity for D2L, D4.2, and 5-HT2A receptors.

Journal: Bioorganic & medicinal chemistry letters 20070315

Title: Synthesis and in vitro binding studies of substituted piperidine naphthamides. Part I: Influence of the substitution on the basic nitrogen and the position of the amide on the affinity for D2L, D4.2, and 5-HT2A receptors.

Journal: Bioorganic & medicinal chemistry letters 20070315

Title: Isolation and characterisation of a Lactobacillus helveticus ITG LH1 peptidase-rich sub-proteome.

Journal: International journal of food microbiology 20051125

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