Chlordimeform

Base Information

• Chemical Name: Chlordimeform
• CAS No.: 6164-98-3
• Molecular Formula: C10H13 Cl N2
• Molecular Weight: 196.68
• Hs Code.: 2925210000
• European Community (EC) Number: 228-200-5
• ICSC Number: 0124
• UN Number: 2588
• UNII: GXA8FP6Y9C
• DSSTox Substance ID: DTXSID2037508
• Nikkaji Number: J3.083J
• Wikipedia: Chlordimeform
• Wikidata: Q415341
• Metabolomics Workbench ID: 55002
• ChEMBL ID: CHEMBL2288609,CHEMBL3186141
• Mol file: 6164-98-3.mol

Synonyms:Chlordimeform;Chlorphenamidine

Chemical Property of Chlordimeform

Chemical Property:

• Vapor Pressure: 0.002mmHg at 25°C
• Melting Point: 32oC
• Refractive Index: nD25 1.5885
• Boiling Point: 163～165
• PKA: 7.89±0.50(Predicted)
• Flash Point: 130.839oC
• PSA: 15.60000
• Density: 1.1
• LogP: 2.86980
• Storage Temp.: 2-8°C
• Water Solubility.: 0.27g/L(20 oC)
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 196.0767261
• Heavy Atom Count: 13
• Complexity: 180

Purity/Quality:

98% ^*data from raw suppliers

Chlordimeform ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn,N
• Hazard Codes: Xn,N
• Statements: 21/22-40-50/53
• Safety Statements: 22-36/37-60-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Other Insecticides
• Canonical SMILES: CC1=C(C=CC(=C1)Cl)N=CN(C)C
• 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.
• Uses: Acaricide, insecticide. Broad-spectrum acaricide used against adult mites, eggs and larvae. Also used as an insecticide against cockroaches, cotton bollworm, cotton budworm, and other pests.

Technology Process of Chlordimeform

There total 3 articles about Chlordimeform 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: 87.0%

4-chloro-2-methylacetanilide (5202-86-8) + N,N-dimethyl-formamide (68-12-2,33513-42-7) → chlordimeform (6164-98-3)

Guidance literature:

With trichlorophosphate; In toluene; at 100 ℃; for 1h;

DOI:10.1055/s-1980-29250

Reference yield:

N,N-dimethyl-formamide (68-12-2,33513-42-7) + 4-chloro-2-methylbenzeneamine (95-69-2) → chlordimeform (6164-98-3)

Guidance literature:

Multistep reaction; (i) SOCl₂, (ii) /BRN= 878505/;

DOI:10.1002/hlca.19730560221

Reference yield:

→ chlordimeform (6164-98-3)

Guidance literature:

DOI:10.1055/s-1979-28757

upstream raw materials:

N,N-dimethyl-formamide

4-chloro-2-methylbenzeneamine

4-chloro-2-methylacetanilide