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Home Amines 582-80-9
582-80-9,MFCD00451153
Catalog No.:AA00ECGA

582-80-9 | 4-(Benzoylamino)benzoic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$17.00   $12.00
- +
1g
95%
in stock  
$45.00   $32.00
- +
10g
98%
in stock  
$411.00   $288.00
- +
25g
98%
in stock  
$760.00   $532.00
- +
100g
98%
in stock  
$2,007.00   $1,405.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00ECGA
Chemical Name:
4-(Benzoylamino)benzoic acid
CAS Number:
582-80-9
Molecular Formula:
C14H11NO3
Molecular Weight:
241.2420
MDL Number:
MFCD00451153
SMILES:
O=C(c1ccccc1)Nc1ccc(cc1)C(=O)O
NSC Number:
74676
Properties
Properties
 
BP:
349.8°C at 760 mmHg  
Form:
Solid  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
302  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
3  
XLogP3:
2.1  

Upstream Synthesis Route

[1]Patent:WO2014/128465,2014,A1,.Locationinpatent:Page/Pagecolumn53

[2]Patent:WO2005/19162,2005,A1,.Locationinpatent:Page/Pagecolumn13-15

[1]BioorganicandMedicinalChemistryLetters,2012,vol.22,#1,p.39-44

[2]Patent:CN106588914,2017,A,.Locationinpatent:Paragraph0172;0176;0177;0178

[3]Patent:CN106588913,2017,A,.Locationinpatent:Paragraph0192;0195;0196;0197

[4]Patent:CN106317057,2017,A,.Locationinpatent:Paragraph0209;0212;0213;0214

[5]Patent:CN107056789,2017,A,.Locationinpatent:Paragraph0183;0186;0187;0188

[1]Patent:US9200142,2015,B2,.Locationinpatent:Page/Pagecolumn50

[2]ActaPoloniaePharmaceutica-DrugResearch,2018,vol.75,#2,p.385-396

[3]SyntheticCommunications,2008,vol.38,#23,p.4068-4075

[4]ChemischeBerichte,1910,vol.43,p.2578

[5]JournaloftheAmericanChemicalSociety,1956,vol.78,p.2570

[6]BulletindelaSocieteChimiquedeFrance,1951,p.220,222

[7]ChemischeBerichte,1910,vol.43,p.2578

[8]JournalofMedicinalChemistry,1988,vol.31,#3,p.590-603

[9]JournalofOrganicChemistryUSSR(EnglishTranslation),1981,vol.17,#11,p.2139-2141

[10]ZhurnalOrganicheskoiKhimii,1981,vol.17,#11,p.2394-2396

[11]RussianJournalofPhysicalChemistryA,1996,vol.70,#12,p.2004-2006

[12]BioorganicandMedicinalChemistryLetters,2012,vol.22,#4,p.1739-1742

[13]JournalofOrganicChemistry,2013,vol.78,#23,p.11765-11771

[1]JournalofOrganicChemistry,2007,vol.72,#3,p.765-774

[1]OrganicLetters,2016,vol.18,#13,p.3114-3117

Downstream Synthesis Route

[1]ChemischeBerichte,1910,vol.43,p.2578

[1]JournalofOrganicChemistry,1989,vol.54,p.3744-3747

[2]JustusLiebigsAnnalenderChemie,1880,vol.205,p.118

108-24-7    582-80-9   
(4-benzoylamino-benzoicacid)-aceticacid-anhydride 

[1]ChemischeBerichte,1910,vol.43,p.2578

[2]ChemischeBerichte,1910,vol.43,p.2578

[1]JournalofOrganicChemistry,1959,vol.24,p.2017

[1]JustusLiebigsAnnalenderChemie,1880,vol.205,p.118

Literature

Title: Design and synthesis of benzoic acid derivatives as influenza neuraminidase inhibitors using structure-based drug design.

Journal: Journal of medicinal chemistry 19971205

Title: Retinobenzoic acids. 1. Structure-activity relationships of aromatic amides with retinoidal activity.

Journal: Journal of medicinal chemistry 19881101

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SDS
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