Home Amines 116-81-4
116-81-4,MFCD00035694
Catalog No.:AA000B9I

116-81-4 | Bromaminic acid

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5g
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$8.00   $6.00
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25g
98%
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$21.00   $15.00
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100g
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$58.00   $41.00
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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:
AA000B9I
Chemical Name:
Bromaminic acid
CAS Number:
116-81-4
Molecular Formula:
C14H8BrNO5S
Molecular Weight:
382.1860
MDL Number:
MFCD00035694
SMILES:
Brc1cc(c(c2c1C(=O)c1ccccc1C2=O)N)S(=O)(=O)O
NSC Number:
7574
Properties
Computed Properties
 
Complexity:
601  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
2.2  

Downstream Synthesis Route

[1]CurrentPatentAssignee:NANTONGZHENGYANPIGMENTCHEMICAL-CN106083660,2016,ALocationinpatent:Paragraph0012

[2]CurrentPatentAssignee:CELANESECORP-US2440760,1944,A

[1]CurrentPatentAssignee:I.G.FARBENINDUSTRIEAG(historic)-DE693610,1937,C[DRP/DRBPOrg.Chem.][DRP/DRBPOrg.Chem.]

[2]CurrentPatentAssignee:GHOLDINGSINC-US2204232,1938,ACurrentPatentAssignee:I.G.FARBENINDUSTRIEAG(historic)-DE693610,1937,C[DRP/DRBPOrg.Chem.][DRP/DRBPOrg.Chem.]

[3]CurrentPatentAssignee:GHOLDINGSINC-US2204232,1938,A

116-81-4    313-12-2   
6-amino-12-trifluoromethyl-13<i>H</i>-naphth2,3-<i>c</i>acridine-5,8,14-trione 

[1]Patent:DE693610,1937,    DRP/DRBPOrg.Chem.,

[2]Patent:US2204232,1938,

[1]CurrentPatentAssignee:BASF-DE287615,1800,C[Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.12,p.478][Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.12,p.478]

[2]CurrentPatentAssignee:AGFA-GEVAERT-DE288665,1800,C[Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.12,p.454][Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.12,p.454]

[1]CurrentPatentAssignee:BASF-DE263395,1800,C[Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.11,p.555][Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.11,p.555]

Literature

Title: Convergent synthesis of the potent P2Y receptor antagonist MG 50-3-1 based on a regioselective Ullmann coupling reaction.

Journal: Molecules (Basel, Switzerland) 20120305

Title: Immobilized laccase on a new cryogel carrier and kinetics of two anthraquinone derivatives oxidation.

Journal: Applied biochemistry and biotechnology 20111201

Title: Structural insights into the inhibition of cytosolic 5'-nucleotidase II (cN-II) by ribonucleoside 5'-monophosphate analogues.

Journal: PLoS computational biology 20111201

Title: Biodegradation of bromoamine acid using combined airlift loop reactor and biological activated carbon.

Journal: Bioresource technology 20110301

Title: Synthesis of alkyl- and aryl-amino-substituted anthraquinone derivatives by microwave-assisted copper(0)-catalyzed Ullmann coupling reactions.

Journal: Nature protocols 20100501

Title: Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases).

Journal: Purinergic signalling 20090301

Title: Influence of Ecto-nucleoside triphosphate diphosphohydrolase activity on Trypanosoma cruzi infectivity and virulence.

Journal: PLoS neglected tropical diseases 20090301

Title: [Degradation characteristics of bromoamine acid by Sphingomonas sp. FL].

Journal: Huan jing ke xue= Huanjing kexue 20080901

Title: The new incorporation bio-treatment technology of bromoamine acid and azo dyes wastewaters under high-salt conditions.

Journal: Biodegradation 20080201

Title: Combinatorial synthesis of anilinoanthraquinone derivatives and evaluation as non-nucleotide-derived P2Y2 receptor antagonists.

Journal: Bioorganic & medicinal chemistry letters 20080101

Title: Rapid and efficient microwave-assisted copper(0)-catalyzed ullmann coupling reaction: general access to anilinoanthraquinone derivatives.

Journal: Organic letters 20070329

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Tags:116-81-4 Molecular Formula|116-81-4 MDL|116-81-4 SMILES|116-81-4 Bromaminic acid