p-Methoxyphenylbiguanide

Base Information

• Chemical Name: p-Methoxyphenylbiguanide
• CAS No.: 43191-41-9
• Molecular Formula: C9H13N5O
• Molecular Weight: 207.235
• NSC Number: 220225
• UNII: XA3020KZD8
• DSSTox Substance ID: DTXSID70195770
• Nikkaji Number: J78.960G
• ChEMBL ID: CHEMBL4077681

Synonyms:43191-41-9;p-Methoxyphenylbiguanide;N-(4-methoxyphenyl)imidodicarbonimidic diamide;1-(diaminomethylidene)-2-(4-methoxyphenyl)guanidine;BIGUANIDE, 1-(p-METHOXYPHENYL)-;Imidodicarbonimidic diamide, N-(4-methoxyphenyl)-;1-(P-methoxyphenyl)-biguanid;NSC 220225;1-(4-methoxyphenyl)biguanide;AI3-51313;XA3020KZD8;CHEMBL4077681;NSC-220225;1-CARBAMIMIDAMIDO-N-(4-METHOXYPHENYL)METHANIMIDAMIDE;UNII-XA3020KZD8;SCHEMBL1742030;DTXSID70195770;1-(P-METHOXYPHENYL)BIGUANIDE;BDBM50227834;CCG-55934;MFCD00448707;NSC220225;STK107041;1-(P-METHOXYPHENYL)BIGUANIDINE;AKOS001184171;LS-06764;LS-43928;CS-0302843;A913672;SR-01000644931-1;Z57275751

Chemical Property of p-Methoxyphenylbiguanide

Chemical Property:

• Vapor Pressure: 9.24E-08mmHg at 25°C
• Boiling Point: 434.8°Cat760mmHg
• Flash Point: 216.7°C
• PSA: 107.01000
• Density: 1.34g/cm³
• LogP: 1.88860
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 207.11201006
• Heavy Atom Count: 15
• Complexity: 251

Purity/Quality:

97% ^*data from raw suppliers

N-(4-Methoxyphenyl)imidodicarbonimidic diamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)N=C(N)N=C(N)N

Technology Process of p-Methoxyphenylbiguanide

There total 3 articles about p-Methoxyphenylbiguanide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

4-methoxy-aniline (104-94-9) + N-Cyanoguanidine (127099-85-8,780722-26-1,461-58-5) → 1-carbamimidamido-N-(4-methoxyphenyl)methanimidamide (43191-41-9)

Guidance literature:

4-methoxy-aniline; N-Cyanoguanidine; With hydrogenchloride; In water; at 90 ℃; for 18h;

at 20 ℃; for 3h;

DOI:10.1016/j.tetlet.2014.10.122

Reference yield:

p-anisidine hydrochloride (20265-97-8) + N-Cyanoguanidine (127099-85-8,780722-26-1,461-58-5) → 1-carbamimidamido-N-(4-methoxyphenyl)methanimidamide (43191-41-9)

Guidance literature:

In ethyl acetate; Heating;

Reference yield:

→ 1-carbamimidamido-N-(4-methoxyphenyl)methanimidamide (43191-41-9)

Guidance literature:

With sodium ethanolate; In ethanol; at 20 ℃; for 3h;

upstream raw materials:

p-anisidine hydrochloride

N-Cyanoguanidine

4-methoxy-aniline

Downstream raw materials:

2-Amino-4-(4-methoxyanilino)-s-triazin

1-(4-methoxy-phenyl)-6,6-dimethyl-1,6-dihydro-[1,3,5]triazine-2,4-diyldiamine; hydrochloride

N-carbamimidoyl-N'-(4-methoxy-phenyl)-urea

N¹-p-Methoxy-phenyl-N⁵-acetoacetylbiguanid

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