Chlordimeform hydrochloride

Base Information

• Chemical Name: Chlordimeform hydrochloride
• CAS No.: 19750-95-9
• Molecular Formula: C10H13ClN2•ClH
• Molecular Weight: 383.643
• European Community (EC) Number: 243-269-1
• UNII: 3YI7CT6416
• ChEMBL ID: CHEMBL3185298
• DSSTox Substance ID: DTXSID5044811
• ICSC Number: 0125
• Wikidata: Q1989088
• Mol file: 19750-95-9.mol

Synonyms:Chlordimeform hydrochloride;19750-95-9;ChlordimeformHydrochloride;Galecron monohydrochloride;DTXSID5044811;Chlordimeform hydrochloride [ISO];19750-95-9 (HCl);Formamidine, N'-(4-chloro-o-tolyl)-N,N-dimethyl-, hydrochloride;3YI7CT6416;N'-(4-Chloro-o-tolyl)-N,N-dimethylformamidine monohydrochloride;SCHEMBL160020;SCHEMBL160021;SPANON MONOHYDROCHLORIDE;SCHEMBL7185165;CHEMBL3185298;DTXCID3024811;Tox21_301412;CHLORPHENAMIDINE MONOHYDROCHLORIDE;NCGC00256207-01;CAS-19750-95-9;NS00082763;J-012762;Q1989088;Chlordimeform hydrochloride, PESTANAL(R), analytical standard;N'-(4-chloro-2-methylphenyl)-N,N-dimethylmethanimidamide;hydrochloride;METHANIMIDAMIDE, N'-(4-CHLORO-2-METHYLPHENYL)-N,N-DIMETHYL-, HYDROCHLORIDE (1:1)

Chemical Property of Chlordimeform hydrochloride

Chemical Property:

• Melting Point: approximate 225℃(dec.)
• Boiling Point: 292.7°Cat760mmHg
• Flash Point: 130.8°C
• PSA: 15.60000
• Density: g/cm³
• LogP: 3.67180
• Storage Temp.: 0-6°C
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 232.0534038
• Heavy Atom Count: 14
• Complexity: 180

Purity/Quality:

Chlordimeform hydrochloride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xn,N
• Statements: 22-40-50/53
• Safety Statements: 22-36/37-60-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC1=C(C=CC(=C1)Cl)N=CN(C)C.Cl
• Inhalation Risk: A harmful concentration of airborne particles can be reached quickly when dispersed.
• Effects of Short Term Exposure: The substance may cause effects on the nervous system. This may result in impaired functions.
• Effects of Long Term Exposure: Repeated or prolonged contact with skin may cause dermatitis. The substance may have effects on the bladder and kidneys. This may result in urinary tract inflammation.

Technology Process of Chlordimeform hydrochloride

There total 2 articles about Chlordimeform hydrochloride 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:

acifluorfen (50594-66-6,94128-04-8) → 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoic acid sodium salt (19750-95-9)

Guidance literature:

With sodium hydroxide; In isopropyl alcohol;

Reference yield:

→ 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoic acid sodium salt (19750-95-9)

Guidance literature:

Reference yield:

sodium salt of 5-(2-chloro-α,α,α-trifluoro-4-tolyloxy)-benzoic acid + 3-(2-chloro-4-(trifluoromethyl)phenoxy)benzoic acid (63734-62-3) + 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoic acid sodium salt (19750-95-9) → acifluorfen (50594-66-6,94128-04-8)

Guidance literature:

With sodium hydroxide; sulfuric acid; nitric acid; In Ac₂ O; water;

upstream raw materials:

acifluorfen

Downstream raw materials:

acifluorfen

Refernces

• 1、 -. "Preparation of 5-(2-halo-4-trifluoromethylphenoxy)-2-nitrobenzoic acid and salts and esters and amides". . . Retrieved 2008/06/13.
• 2、 -. "Herbicidal 4-trifluoromethyl-3'-nitrogen-substituted-4'-substituted diphenyl ethers". . . Retrieved 2008/06/13.