1,2-Dibromo-4-(1,2-dibromoethyl)cyclohexane

Base Information

• Chemical Name: 1,2-Dibromo-4-(1,2-dibromoethyl)cyclohexane
• CAS No.: 3322-93-8
• Molecular Formula: C8H12 Br4
• Molecular Weight: 427.799
• Hs Code.: 2903890090
• European Community (EC) Number: 222-036-8
• UNII: 502D5Q149T
• DSSTox Substance ID: DTXSID8024947
• Nikkaji Number: J205.407H
• Wikidata: Q20054503
• Pharos Ligand ID: NA7XZDDYTS5M
• ChEMBL ID: CHEMBL375107
• Mol file: 3322-93-8.mol

Synonyms:1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane;BCH cyclohexane compound;TBECH cpd

Chemical Property of 1,2-Dibromo-4-(1,2-dibromoethyl)cyclohexane

Chemical Property:

• Vapor Pressure: 2.23E-05mmHg at 25°C
• Melting Point: 72-73℃ (ethyl ether )
• Refractive Index: 1.7040 (estimate)
• Boiling Point: 371.2°Cat760mmHg
• Flash Point: 173.3°C
• PSA: 0.00000
• Density: 2.17g/cm³
• LogP: 4.47190
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility.: Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Slightly)
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 2
• Exact Mass: 427.76315
• Heavy Atom Count: 12
• Complexity: 139

Purity/Quality:

99%, ^*data from raw suppliers

1,2-Dibromo-4-(1,2-dibromoethyl)cyclohexane ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Plastics & Rubber -> Other Plasticizers
• Canonical SMILES: C1CC(C(CC1C(CBr)Br)Br)Br
• Uses: Tetrabromoethylcyclohexane (TBECH) is an additive brominated flame retardant used in domestic and industrial applications. It was used to investigate the biodegradation kinetics in aerobic and anaerob ic soil. Tetrabromoethylcyclohexane (TBECH) is an additive brominated flame retardant used in domestic and industrial applications. It was used to investigate the biodegradation kinetics in aerobic and anaerobic soil.

Technology Process of 1,2-Dibromo-4-(1,2-dibromoethyl)cyclohexane

There total 5 articles about 1,2-Dibromo-4-(1,2-dibromoethyl)cyclohexane 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-ethenylcyclohexene (100-40-3) → BCH (3322-93-8)

Guidance literature:

With potassium permanganate; hydrogen bromide; In acetonitrile;

DOI:10.1002/jccs.199600010

Reference yield:

4-ethenylcyclohexene (100-40-3) → BCH (3322-93-8)

Guidance literature:

With diethyl ether; bromine; at -18 ℃; lower-melting 3.4-dibromo-1-<1.2-dibromo-ethyl>-cyclohexane;

Reference yield:

4-ethenylcyclohexene (100-40-3) → BCH (3322-93-8)

Guidance literature:

With diethyl ether; bromine; at -18 ℃; higher-melting 3.4-dibromo-1-<1.2-dibromo-ethyl>-cyclohexane;

upstream raw materials:

4-ethenylcyclohexene

Downstream raw materials:

4-ethenylcyclohexene

4-(1,2-Dibromo-ethyl)-cyclohexene

Refernces