Catalog No.:AA0032P3

4023-02-3 | 1H-Pyrazole-1-carboxamidine, HCl

Name: Name:1H-Pyrazole-1-carboxamidine, HCl
Brand: AABLOCKS
SKU: AA0032P3
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10g

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25g

97%

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$11.00 $8.00

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100g

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500g

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

Technical Information

Catalog Number:

AA0032P3

Chemical Name:

1H-Pyrazole-1-carboxamidine, HCl

CAS Number:

4023-02-3

Molecular Formula:

C4H7ClN4

Molecular Weight:

146.5782

MDL Number:

MFCD00210087

SMILES:

NC(=N)n1cccn1.Cl

Properties

Form:

Solid

MP:

167-170 °C(lit.)

Storage:

Inert atmosphere;Room Temperature;

Computed Properties

Complexity:

100

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

Upstream Synthesis Route

288-13-1

420-04-2

4023-02-3

[1]JournalofOrganicChemistry,1992,vol.57,#8,p.2497-2502

[2]OrganicLetters,2004,vol.6,#26,p.4925-4927

[3]Patent:KR101808950,2017,B1,.Locationinpatent:Paragraph0233-0236

[4]BioorganicandMedicinalChemistryLetters,2000,vol.10,#24,p.2771-2774

[5]JournalofMedicinalChemistry,2005,vol.48,#3,p.812-820

102-52-3

2582-30-1

4023-02-3

[1]JournaloftheAmericanChemicalSociety,2010,vol.132,#32,p.11223-11233

420-04-2

35877-22-6

4023-02-3

[1]TetrahedronLetters,2004,vol.45,#51,p.9423-9426

102-52-3

1937-19-5

4023-02-3

[1]JournalofMedicinalChemistry,2008,vol.51,#24,p.8168-8172

24424-99-5

4023-02-3

152120-61-1

[1]TetrahedronLetters,2007,vol.48,#13,p.2357-2359

[2]OrganicandBiomolecularChemistry,2013,vol.11,#24,p.3943-3948

[3]Patent:WO2015/147950,2015,A2,.Locationinpatent:Page/Pagecolumn38

[4]Patent:US2013/79324,2013,A1,.Locationinpatent:Paragraph0827;0828

[5]TetrahedronLetters,1993,vol.34,#21,p.3389-3392

[6]Tetrahedron,2007,vol.63,#38,p.9502-9513

[7]Patent:EP945138,1999,A1,

Downstream Synthesis Route

24424-99-5

4023-02-3

152120-61-1

[1]TetrahedronLetters,2007,vol.48,p.2357-2359

[2]OrganicandBiomolecularChemistry,2013,vol.11,p.3943-3948

[3]Patent:WO2015/147950,2015,A2.Locationinpatent:Page/Pagecolumn38

[4]Patent:US2013/79324,2013,A1.Locationinpatent:Paragraph0827;0828

[5]TetrahedronLetters,1993,vol.34,p.3389-3392

[6]Tetrahedron,2007,vol.63,p.9502-9513

[7]Patent:EP945138,1999,A1

108-91-8

4023-02-3

2498-47-7

[1]Fujita,Mitsue;Furusho,Yoshio[Tetrahedron,2018,vol.74,#32,p.4339-4342]

[2]An,Taeyang;Lee,Yan[OrganicLetters,2021,vol.23,#23,p.9163-9167]

[3]An,Taeyang;Kang,Byeongwoo;Kang,Sunyoung;Pac,Jinyoung;Youk,Jihea;Lin,Dian;Lee,Yan[ChemicalCommunications,2019,vol.55,#69,p.10222-10225]

[4]Bernatowicz,MichaelS.;Wu,Youling;Matsueda,GaryR.[JournalofOrganicChemistry,1992,vol.57,#8,p.2497-2502]

[5]Solomin,VitaliiV.;Seins,Alberts;Jirgensons,Aigars[Synlett,2020,vol.31,#15,p.1507-1510]

501-53-1

4023-02-3

152120-62-2

[1]TetrahedronLetters,1993,vol.34,p.3389-3392

[2]JournalofMedicinalChemistry,2008,vol.51,p.8168-8172

29390-67-8

4023-02-3

mono-6-deoxy-6-guanidinocycloheptaamylose

[1]JournaloftheAmericanChemicalSociety,2018,vol.140,p.3959-3974

[2]JournalofOrganicChemistry,1998,vol.63,p.1737-1739

62234-37-1

4023-02-3

Nα-benzyloxycarbonyl-β-guanidino-D-α-alanine

[1]Tetrahedron,2000,vol.56,p.2513-2522

Literature

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