HomeProductsBuilding BlocksFunctional GroupsKetones2-Acetylcyclohexanone
Chemical structure of CAS 874-23-7

2-Acetylcyclohexanone

In Stock•Starting at $8 for 1 g•Purity ≥ 98%
CAS No.874-23-7
MDL No.MFCD00001633
MFC8H12O2
MW140.18
InChI KeyOEKATORRSPXJHE-UHFFFAOYSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
1 g98%$8In Stock
5 g98%$9In Stock
10 g98%$13In Stock
25 g98%$24In Stock
100 g98%$84In Stock
500 g98%$403In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

CAS No.874-23-7
Product Name2-Acetylcyclohexanone
Heavy Atom Count10Rotatable Bond Count1
Atom Stereo Count1Bond Stereo Count0
HBA2HBD0
TPSA34.140 ŲCharge0
Exact Mass140.08373Complexity160.64
pKa7.765XLogP1.335

Related Articles

Studies related to this compound and its mechanism of action

Allergic contact dermatitis: epidemiology, molecular mechanisms, in vitro methods and regulatory aspects. Current knowledge assembled at an international workshop at BfR, Germany.

Cellular and molecular life sciences : CMLS • Vol. 69, Issue 5 • 2012
PMID: 21997384PMC: PMC3276771DOI: 10.1007/s00018-011-0846-8

8-Azatetracyclines: synthesis and evaluation of a novel class of tetracycline antibacterial agents.

Journal of medicinal chemistry • Vol. 54, Issue 5 • 2011
PMID: 21302930PMC: PMC3103189DOI: 10.1021/jm1015389

Copper-catalyzed amination of (bromophenyl)ethanolamine for a concise synthesis of aniline-containing analogues of NMDA NR2B antagonist ifenprodil.

Organic & biomolecular chemistry • Vol. 8, Issue 5 • 2010
PMID: 20165802DOI: 10.1039/b923255a

Tautomerization of 2-acetylcyclohexanone. 1. Characterization of keto-enol/enolate equilibria and reaction rates in water.

The Journal of organic chemistry • Vol. 68, Issue 7 • 2003
PMID: 12662038DOI: 10.1021/jo026629x

Documentation

Similar Products