Bromociclen

Base Information

• Chemical Name: Bromociclen
• CAS No.: 1715-40-8
• Molecular Formula: C8H5 Br Cl6
• Molecular Weight: 393.75
• Hs Code.: 2903890090
• European Community (EC) Number: 216-996-7
• DSSTox Substance ID: DTXSID6041680
• Nikkaji Number: J7.572H
• Wikidata: Q27155747
• NCI Thesaurus Code: C74161
• ChEMBL ID: CHEMBL1437390
• Mol file: 1715-40-8.mol

Synonyms:5-bromomethyl-1,2,3,4,7,7-hexachloro-bicyclo(2,2,1)heptene;bromocyclen

Chemical Property of Bromociclen

Chemical Property:

• Vapor Pressure: 2E-05mmHg at 25°C
• Boiling Point: 372.8 °C at 760 mmHg
• Flash Point: 206.5 °C
• PSA: 39.33000
• Density: 1.95 g/cm³
• LogP: 0.30500
• XLogP3: 4.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 391.76763
• Heavy Atom Count: 15
• Complexity: 353

Purity/Quality:

99.9% ^*data from raw suppliers

Bromodan-d5 ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Low toxicity by ingestion.
• Hazard Codes: Low toxicity by ingestion.

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(C2(C(=C(C1(C2(Cl)Cl)Cl)Cl)Cl)Cl)CBr
• Uses: Name previously used: Bromocyclen.

Technology Process of Bromociclen

There total 7 articles about Bromociclen 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:

Ethylenglykol-bis-di-<1,4,5,6,7,7-hexachlor-norbornenyl-(2)>-methylether (110029-52-2) → 5-(bromomethyl)-1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-ene (1715-40-8)

Guidance literature:

With hydrogen bromide; acetic acid;

DOI:10.1007/BF00903168

Reference yield:

allyl bromide (106-95-6) + hexachlorocyclopentadiene (77-47-4) → 5-(bromomethyl)-1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-ene (1715-40-8)

Guidance literature:

DOI:10.1007/BF00903168

Reference yield:

allyl bromide (106-95-6) + hexachlorocyclopentadiene (77-47-4) → Bromodan (1715-40-8,17442-37-4)

Guidance literature:

DOI:10.1021/ja01639a034 DOI:10.1021/ja01621a082 DOI:10.1007/BF00903168

upstream raw materials:

Ethylenglykol-bis-di-<1,4,5,6,7,7-hexachlor-norbornenyl-(2)>-methylether

allyl bromide

hexachlorocyclopentadiene

1,2,3,4,7,7-hexachloro-5-methyleno-2-norbornene