Catalog No.:AA0033N3

38235-71-1 | 3-Hydrazinobenzoic acid

Name: Name:3-Hydrazinobenzoic acid
Brand: AABLOCKS
SKU: AA0033N3
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25g

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA0033N3

Chemical Name:

3-Hydrazinobenzoic acid

CAS Number:

38235-71-1

Molecular Formula:

C7H8N2O2

Molecular Weight:

152.1506

MDL Number:

MFCD00191447

SMILES:

NNc1cccc(c1)C(=O)O

Properties

BP:

387.6°C at 760 mmHg

Form:

Solid

MP:

191-194 °C

Storage:

Inert atmosphere;-20 ℃;

Computed Properties

Complexity:

149

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

-0.9

Downstream Synthesis Route

99-05-8

38235-71-1

[1]CurrentPatentAssignee:NOVOGENLTD-WO2016/8010,2016,A1Locationinpatent:Page/Pagecolumn38

[2]Griess[JustusLiebigsAnnalenderChemie,1861,vol.120,p.126][ChemischeBerichte,1876,vol.9,p.1657]Roder[JustusLiebigsAnnalenderChemie,1886,vol.236,p.164]

[3]Locationinpatent:schemeortableBowers,ErinM.;Yan,Gai;Mukherjee,Chandrani;Orry,Andrew;Wang,Ling;Holbert,MarcA.;Crump,NicholasT.;Hazzalin,CatherineA.;Liszczak,Glen;Yuan,Hua;Larocca,Cecilia;Saldanha,S.Adrian;Abagyan,Ruben;Sun,Yan;Meyers,DavidJ.;Marmorstein,Ronen;Mahadevan,LouisC.;Alani,RhodaM.;Cole,PhilipA.[ChemistryandBiology,2010,vol.17,#5,p.471-482]

[4]Zhou,Xia;Tan,Yuping;Gou,Kun;Tao,Lei;Luo,Yuan;Zhou,Yue;Zuo,Zeping;Sun,Qingxiang;Luo,Youfu;Zhao,Yinglan[BioorganicChemistry,2021,vol.115]

38235-71-1

88174-23-6

(E)-3-{2-(2,6-dibromo-4-methylphenyl)methylidenehydrazino}benzoicacid

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-WO2007/122165,2007,A1Locationinpatent:Page/Pagecolumn55-56

108-94-1

38235-71-1

729613-71-2

[1]CurrentPatentAssignee:NOVOGENLTD-WO2016/8010,2016,A1Locationinpatent:Page/Pagecolumn38;39

[2]CurrentPatentAssignee:SWEDISHORPHANBIOVITRUMAB-WO2004/63156,2004,A1Locationinpatent:Page41

[3]Locationinpatent:schemeortableBarf,Tjeerd;Lehmann,Fredrik;Hammer,Kristin;Haile,Saba;Axen,Eva;Medina,Carmen;Uppenberg,Jonas;Svensson,Stefan;Rondahl,Lena;Lundbaeck,Thomas[BioorganicandMedicinalChemistryLetters,2009,vol.19,#6,p.1745-1748]

455-19-6

1948-40-9

2973-77-5

10203-08-4

447-61-0

619-21-6

454-89-7

32085-88-4

39943-56-1

83-38-5

619-67-0

100-52-7

619-66-9

38235-71-1

100-63-0

368-78-5

365-34-4

119-67-5

14763-24-7

5326-27-2

74478-58-3

588-64-7

3-(phenyl-hydrazonomethyl)-benzoicacid

N-(2,6-Dichloro-phenyl)-N'-1-(3,5-dichloro-phenyl)-meth-(E)-ylidene-hydrazine

N-(2,6-Dichloro-phenyl)-N'-1-(3,5-difluoro-phenyl)-meth-(E)-ylidene-hydrazine

C15H12N2O4

N-(3,5-Dichloro-phenyl)-N'-1-(2-trifluoromethyl-phenyl)-meth-(E)-ylidene-hydrazine

N-(3,5-Dichloro-phenyl)-N'-1-(4-trifluoromethyl-phenyl)-meth-(E)-ylidene-hydrazine

C15H12N2O4

N-(2,6-Dichloro-phenyl)-N'-1-(4-trifluoromethyl-phenyl)-meth-(E)-ylidene-hydrazine

C15H12N2O4

N-(2,6-Dichloro-phenyl)-N'-1-(3-trifluoromethyl-phenyl)-meth-(E)-ylidene-hydrazine

N-(3,5-Dichloro-phenyl)-N'-1-(3-trifluoromethyl-phenyl)-meth-(E)-ylidene-hydrazine

C15H12N2O4

N-(3-Trifluoromethyl-phenyl)-N'-1-(3-trifluoromethyl-phenyl)-meth-(E)-ylidene-hydrazine

N-(2-Trifluoromethyl-phenyl)-N'-1-(2-trifluoromethyl-phenyl)-meth-(E)-ylidene-hydrazine

4-{N'-1-(3,5-Dibromo-4-hydroxy-phenyl)-meth-(E)-ylidene-hydrazino}-benzoicacid

N-(3-Trifluoromethyl-phenyl)-N'-1-(2-trifluoromethyl-phenyl)-meth-(E)-ylidene-hydrazine

2,6-dibromo-4-(3-trifluoromethyl-phenyl)-hydrazonomethyl-phenol

2,6-dibromo-4-(2-trifluoromethyl-phenyl)-hydrazonomethyl-phenol

4-{N'-1-(4-Hydroxy-3,5-diiodo-phenyl)-meth-(E)-ylidene-hydrazino}-benzoicacid

3-{N'-1-(4-Hydroxy-3,5-diiodo-phenyl)-meth-(E)-ylidene-hydrazino}-benzoicacid

2,6-diiodo-4-(2-trifluoromethyl-phenyl)-hydrazonomethyl-phenol

[1]Patent:US2006/178527,2006,A1.Locationinpatent:Page/Pagecolumn4

etherealhydrogenchloride

40594-34-1

38235-71-1

60480-92-4

[1]Patent:US3959309,1976,A

[2]Patent:US4062864,1977,A

Literature

Title: Small-molecule inhibitor leads of ribosome-inactivating proteins developed using the doorstop approach.

Journal: PloS one 20110101

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