(Bromomethyl)cyclopentane

Base Information

• Chemical Name: (Bromomethyl)cyclopentane
• CAS No.: 3814-30-0
• Molecular Formula: C6H11Br
• Molecular Weight: 163.057
• Hs Code.: 2903890090
• DSSTox Substance ID: DTXSID20508114
• Nikkaji Number: J2.901.797B
• Wikidata: Q72446994
• Mol file: 3814-30-0.mol

Synonyms:(bromomethyl)cyclopentane;3814-30-0;bromomethylcyclopentane;Cyclopentylmethyl bromide;bromomethyl cyclopentane;MFCD09263483;CYCLOPENTANE, (BROMOMETHYL)-;bromomethyl-cyclopentane;BROMOCYCLOPENTYLMETHANE;cyclopentylmethylbromide;1-(bromomethyl)cyclopentane;SCHEMBL7846;AMY6992;DTXSID20508114;XYZUWOHEILWUID-UHFFFAOYSA-N;(Bromomethyl)cyclopentane, AldrichCPR;AKOS005260295;AB50196;CS-W004985;B6314;FT-0650408;EN300-41645;A824026;J-519950;F1905-0016

Chemical Property of (Bromomethyl)cyclopentane

Chemical Property:

• Appearance/Colour: colorless or light yellow liquid
• Vapor Pressure: 4.174mmHg at 25°C
• Refractive Index: 1.489
• Boiling Point: 153.954 °C at 760 mmHg
• Flash Point: 58.813 °C
• PSA: 0.00000
• Density: 1.326 g/cm₃
• LogP: 2.57150
• Storage Temp.: Inert atmosphere,Room Temperature
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 162.00441
• Heavy Atom Count: 7
• Complexity: 46.1

Purity/Quality:

98%,99%, ^*data from raw suppliers

Bromomethylcyclopentane ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 25
• Safety Statements: 45

MSDS Files:

Useful:

• Canonical SMILES: C1CCC(C1)CBr

Technology Process of (Bromomethyl)cyclopentane

There total 4 articles about (Bromomethyl)cyclopentane 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:

bicyclo[3.1.0]hexane (285-58-5) → 1-bromocyclohexane (108-85-0) + cyclopentylmethyl bromide (3814-30-0) + cis-1,3-dibromocyclohexane (31025-70-4) + trans-1,3-dibromocyclohexane (29624-17-7)

Guidance literature:

With bromine; In tetrachloromethane; at 20 ℃; Yield given. Further byproducts given. Yields of byproduct given; Irradiation;

Reference yield:

1-amino-cyclopentanemethanol (3637-61-4) → 1-bromocyclohexane (108-85-0) + cyclopentylmethyl bromide (3814-30-0)

Guidance literature:

With phosphorus tribromide;

DOI:10.1021/jo01118a033

Reference yield:

bicyclo[3.1.0]hexane (285-58-5) → 1-bromocyclohexane (108-85-0) + 2-methylbromocyclopentane (31201-11-3) + 1-bromo-2-bromomethyl-cyclopentane (861316-92-9) + cyclopentylmethyl bromide (3814-30-0) + cis-1,3-dibromocyclohexane (31025-70-4) + trans-1,3-dibromocyclohexane (29624-17-7)

Guidance literature:

With bromine; In tetrachloromethane; at 20 ℃; Product distribution; Mechanism; Irradiation;

upstream raw materials:

1-amino-cyclopentanemethanol

bicyclo[3.1.0]hexane

phosphorus tribromide

Downstream raw materials:

4-ethoxy-2-phenylquinoline

1-(3-benzyloxyphenyl)-2-cyclopentylethanone

Methyl 3-cyclopentyl-2-methyl-2-phenylpropanoate

1-[2-(cyclopentylmethoxy)phenyl]-3-methyl-2,5,6,7-tetrahydro-4H-isoindol-4-one

Refernces