2,5-Diamino-3-chlorobenzonitrile

Base Information

• Chemical Name: 2,5-Diamino-3-chlorobenzonitrile
• CAS No.: 82997-64-6
• Molecular Formula: C7H6ClN3
• Molecular Weight: 167.598
• Hs Code.: 2926909090
• DSSTox Substance ID: DTXSID70549835
• Wikidata: Q82428987
• Mol file: 82997-64-6.mol

Synonyms:2,5-DIAMINO-3-CHLOROBENZONITRILE;82997-64-6;SCHEMBL2435542;DTXSID70549835;VXWZNVZGPHXSRL-UHFFFAOYSA-N;2,5-Diamino-3-chloro-benzonitrile;MFCD08704820;AKOS006288325;AB48593;CS-0364960;ETHYL2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE

Chemical Property of 2,5-Diamino-3-chlorobenzonitrile

Chemical Property:

• PSA: 75.83000
• LogP: 2.53848
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 167.0250249
• Heavy Atom Count: 11
• Complexity: 185

Purity/Quality:

98%min ^*data from raw suppliers

2,5-Diamino-3-chlorobenzonitrile ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(C=C(C(=C1C#N)N)Cl)N

Technology Process of 2,5-Diamino-3-chlorobenzonitrile

There total 1 articles about 2,5-Diamino-3-chlorobenzonitrile 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: 99.0%

1-amino-2-cyano-4-nitro-6-chlorobenzene (20352-84-5) → 2-chloro-6-cyano-p-phenylenediamine (82997-64-6)

Guidance literature:

With hydrogenchloride; zinc; In tetrahydrofuran; water; for 2h;

Reference yield: 91.0%

1,1'-oxybis(2-bromo-ethane) (5414-19-7) + 2-chloro-6-cyano-p-phenylenediamine (82997-64-6) → 2-amino-3-chloro-5-morpholin-4-yl-benzonitrile

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In DMF (N,N-dimethyl-formamide); at 180 ℃; for 0.5h;

Reference yield: 46.0%

2-chloro-6-cyano-p-phenylenediamine (82997-64-6) + benzenesulfenyl chloride (931-59-9) → C19H12ClN3S2

Guidance literature:

With pyridine; In dichloromethane;

upstream raw materials:

1-amino-2-cyano-4-nitro-6-chlorobenzene