5614-37-9,MFCD08276401
Catalog No.:AA003526

5614-37-9 | Methoxycyclopentane

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$27.00   $19.00
- +
25g
98%
in stock  
$43.00   $30.00
- +
100g
98%
in stock  
$75.00 $53.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003526
Chemical Name:
Methoxycyclopentane
CAS Number:
5614-37-9
Molecular Formula:
C6H12O
Molecular Weight:
100.1589
MDL Number:
MFCD08276401
SMILES:
COC1CCCC1
Properties
Properties
 
BP:
106°C  
Form:
Liquid  
MP:
-140°C  
Refractive Index:
1.421  
Storage:
2-8℃;  

Computed Properties
 
Complexity:
46.1  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.3  

Literature

Title: Ring-expansion reaction of oximes with aluminum reductants.

Journal: Molecules (Basel, Switzerland) 20120614

Title: Cyclopentyl methyl ether: an alternative solvent for palladium-catalyzed direct arylation of heteroaromatics.

Journal: ChemSusChem 20110418

Title: Recycling the tert-butanesulfinyl group in the synthesis of amines using tert-butanesulfinamide.

Journal: The Journal of organic chemistry 20090403

Title: 2-Methoxycyclopentyl analogues of a Pseudomonas aeruginosa quorum sensing modulator.

Journal: Molecular bioSystems 20080601

Title: Practical and robust method for regio- and stereoselective preparation of (E)-ketene tert-butyl TMS acetals and beta-ketoester-derived tert-butyl (1Z,3E)-1,3-bis(TMS)dienol ethers.

Journal: The Journal of organic chemistry 20071012

Title: Highly enantioselective phase-transfer-catalyzed alkylation of protected alpha-amino acid amides toward practical asymmetric synthesis of vicinal diamines, alpha-amino ketones, and alpha-amino alcohols.

Journal: Journal of the American Chemical Society 20050413

Title: Enhancement of enzyme activity and enantioselectivity by cyclopentyl methyl ether in the transesterification catalyzed by Pseudomonas cepacia lipase co-lyophilized with cyclodextrins.

Journal: Biotechnology letters 20050301

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SDS
Tags:5614-37-9 Molecular Formula|5614-37-9 MDL|5614-37-9 SMILES|5614-37-9 Methoxycyclopentane
Catalog No.: AA003526
5614-37-9,MFCD08276401
5614-37-9 | Methoxycyclopentane
Pack Size: 5g
Purity: 98%
in stock
$27.00 $19.00
Pack Size: 25g
Purity: 98%
in stock
$43.00 $30.00
Pack Size: 100g
Purity: 98%
in stock
$75.00 $53.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003526
Chemical Name: Methoxycyclopentane
CAS Number: 5614-37-9
Molecular Formula: C6H12O
Molecular Weight: 100.1589
MDL Number: MFCD08276401
SMILES: COC1CCCC1
Properties
BP: 106°C  
Form: Liquid  
MP: -140°C  
Refractive Index: 1.421  
Storage: 2-8℃;  
Complexity: 46.1  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 7  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.3  
Literature fold

Title: Ring-expansion reaction of oximes with aluminum reductants.

Journal: Molecules (Basel, Switzerland)20120614

Title: Cyclopentyl methyl ether: an alternative solvent for palladium-catalyzed direct arylation of heteroaromatics.

Journal: ChemSusChem20110418

Title: Recycling the tert-butanesulfinyl group in the synthesis of amines using tert-butanesulfinamide.

Journal: The Journal of organic chemistry20090403

Title: 2-Methoxycyclopentyl analogues of a Pseudomonas aeruginosa quorum sensing modulator.

Journal: Molecular bioSystems20080601

Title: Practical and robust method for regio- and stereoselective preparation of (E)-ketene tert-butyl TMS acetals and beta-ketoester-derived tert-butyl (1Z,3E)-1,3-bis(TMS)dienol ethers.

Journal: The Journal of organic chemistry20071012

Title: Highly enantioselective phase-transfer-catalyzed alkylation of protected alpha-amino acid amides toward practical asymmetric synthesis of vicinal diamines, alpha-amino ketones, and alpha-amino alcohols.

Journal: Journal of the American Chemical Society20050413

Title: Enhancement of enzyme activity and enantioselectivity by cyclopentyl methyl ether in the transesterification catalyzed by Pseudomonas cepacia lipase co-lyophilized with cyclodextrins.

Journal: Biotechnology letters20050301

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