3,5-Dichloro-N-hydroxy-benzamidine

Base Information

• Chemical Name: 3,5-Dichloro-N-hydroxy-benzamidine
• CAS No.: 22179-81-3
• Molecular Formula: C7H6 Cl2 N2 O
• Molecular Weight: 205.043
• Hs Code.: 2925290090
• Mol file: 22179-81-3.mol

Synonyms:3,5-DICHLORO-N-HYDROXY-BENZAMIDINE;3,5-Dichloro-N-hydroxybenzimidamide;22179-81-3;3,5-DICHLORO-N'-HYDROXYBENZIMIDAMIDE;SCHEMBL17730391;3,5-dichloro-n-hydroxybenzamidine;HMS1451P12;IDI1_018769;(E)-3,5-dichloro-N'-hydroxybenzimidamide;CS-0437032;EN300-1291438;3,5-dichloro-N'-hydroxybenzene-1-carboximidamide

Chemical Property of 3,5-Dichloro-N-hydroxy-benzamidine

Chemical Property:

• PSA: 58.61000
• LogP: 2.78820
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 203.9857182
• Heavy Atom Count: 12
• Complexity: 176

Purity/Quality:

97% ^*data from raw suppliers

3,5-Dichloro-N-hydroxybenzimidamide 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(C=C(C=C1Cl)Cl)C(=NO)N
• Isomeric SMILES: C1=C(C=C(C=C1Cl)Cl)/C(=N/O)/N

Technology Process of 3,5-Dichloro-N-hydroxy-benzamidine

There total 2 articles about 3,5-Dichloro-N-hydroxy-benzamidine 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: 85.1%

3,5-dichlorobenzonitrile (6575-00-4) → 3,5-dichloro-N'-hydroxybenzenecarboximidamide (22179-81-3)

Guidance literature:

With hydroxylamine hydrochloride; sodium carbonate; In ethanol; water; at 70 ℃; for 8h;

DOI:10.1002/cbdv.201800599

Reference yield:

→ 3,5-dichloro-N'-hydroxybenzenecarboximidamide (22179-81-3)

Guidance literature:

3,5-Dichlor-thiobenzamid, NH2OH ;

DOI:10.1039/j39690000861

Reference yield: 38.5%

3,5-dichloro-N'-hydroxybenzenecarboximidamide (22179-81-3) + 1‐(4‐methoxybenzyl)‐6‐[(4‐methoxybenzyl)oxy]‐3‐(trifluoromethyl)‐1H‐pyrazolo[3,4‐b]pyridine‐5‐carboxylic acid → 3‐(3,5‐dichlorophenyl)‐5‐{1‐(4‐methoxybenzyl)‐6‐[(4‐methoxybenzyl)oxy]‐3‐(trifluoromethyl)‐1H‐pyrazolo[3,4‐b]pyridin‐5‐yl}‐1,2,4‐oxadiazole

Guidance literature:

1‐(4‐methoxybenzyl)‐6‐[(4‐methoxybenzyl)oxy]‐3‐(trifluoromethyl)‐1H‐pyrazolo[3,4‐b]pyridine‐5‐carboxylic acid; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;

3,5-dichloro-N'-hydroxybenzenecarboximidamide; In N,N-dimethyl-formamide; at 20 ℃; for 120h;

DOI:10.1002/ardp.202000458

upstream raw materials:

3,5-dichlorobenzonitrile

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