Cyclopentanemethanol

Base Information

• Chemical Name: Cyclopentanemethanol
• CAS No.: 3637-61-4
• Molecular Formula: C6H12O
• Molecular Weight: 100.161
• Hs Code.: 29061990
• European Community (EC) Number: 222-861-3
• NSC Number: 102763
• UNII: 4LG8NG324P
• DSSTox Substance ID: DTXSID70189896
• Nikkaji Number: J45.675F
• Wikidata: Q63408934
• Mol file: 3637-61-4.mol

Synonyms:Cyclopentanemethanol;Cyclopentylmethanol;3637-61-4;CyclopentYl-Methanol;Cyclopentylcarbinol;Cyclopentyl carbinol;Cyclopentylmethyl alcohol;MFCD00001384;(Hydroxymethyl)cyclopentane;AI3-28356;4LG8NG324P;EINECS 222-861-3;NSC-102763;1198600-13-3;cyclopentanmethanol;cylcopentanemethanol;cyclopentan-methanol;cyclopentyl methanol;cyclo-pentanemethanol;cyclopentane methanol;cyclopentane-methanol;NSC102763;(cyclopentyl)methanol;Cyclopentanemethan-1-ol;Cyclopentanemethanol, 98%;SCHEMBL5625;UNII-4LG8NG324P;DTXSID70189896;BCP29184;AKOS009157998;CS-W001923;DS-1149;NSC 102763;PB47523;PS-9322;SY006011;AM20090579;BB 0221114;C2658;FT-0624251;EN300-49287;W-106621;Q63408934;F0001-1040;Z397587414

Chemical Property of Cyclopentanemethanol

Chemical Property:

• Appearance/Colour: Clear colourless liquid
• Vapor Pressure: 0.721mmHg at 25°C
• Melting Point: 121-123 °C(Solv: hexane (110-54-3))
• Refractive Index: n20/D 1.458(lit.)
• Boiling Point: 162.999 °C at 760 mmHg
• PKA: 15.26±0.10(Predicted)
• Flash Point: 62.222 °C
• PSA: 20.23000
• Density: 0.934 g/cm³
• LogP: 1.16890
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 100.088815002
• Heavy Atom Count: 7
• Complexity: 46.1

Purity/Quality:

99.9% ^*data from raw suppliers

Cyclopentanemethanol ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 23-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC(C1)CO
• Uses: Cyclopentanemethanol was used to study catalytic reduction of 6-bromo-1-hexene by nickel (I) salen electrogenerated at a glassy carbon electrode in acetonitrile containing tetramethylammonium tetrafluoroborate by cyclic voltammetry and controlled-potential electrolysis.

Technology Process of Cyclopentanemethanol

There total 72 articles about Cyclopentanemethanol 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: 99.0%

cyclopentylmethyl acetate (26600-49-7) → 1-amino-cyclopentanemethanol (3637-61-4)

Guidance literature:

With methanol; potassium permanganate; trimethylsulphonium iodide; at 25 ℃; under 760.051 Torr; chemoselective reaction;

DOI:10.1039/d1ra03209g

Reference yield: 98.0%

Cyclopentylmethoxy-trimethyl-silane (122424-46-8) → 1-amino-cyclopentanemethanol (3637-61-4)

Guidance literature:

With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate; at 20 ℃; for 0.0833333h; Green chemistry;

DOI:10.1016/j.molcata.2012.08.002

Reference yield: 95.0%

cyclopentanealdehyde (872-53-7) → 1-amino-cyclopentanemethanol (3637-61-4)

Guidance literature:

In toluene; at 25 ℃; for 48h;

DOI:10.1016/j.tet.2011.08.063

upstream raw materials:

formaldehyd

cyclopentylmagnesium chloride

cyclopentanealdehyde

ethanol

Downstream raw materials:

cyclopentamethyl phenyl N-methyl-N-(2-chloroethyl)phosphoramidate

cyclopentamethyl phenyl N-methyl-N-(2-bromoethyl)phosphoramidate

cyclopentamethyl phenyl N,N-bis(2-bromoethyl)phosphoramidate

4-Chloro-benzenesulfonic acid cyclopentylmethyl ester

Refernces

• 1、 Cao, Ji,Gan, Jianxing,Hacatrjan, Schanth,Liu, Lujie,Nakagawa, Yoshinao,Tamura, Masazumi,Tomishige, Keiichi,Yabushita, Mizuho. "Titania-supported molybdenum oxide combined with Au nanoparticles as a hydrogen-driven deoxydehydration catalyst of diol compounds". . p. 2146 - 2161. Retrieved 2022/04/28.
• 2、 -. "ATF6 MODULATORS AND USES THEREOF". Paragraph 249. . Retrieved 2021/04/17.