HomeProductsBuilding BlocksOrganic Building BlocksBenzene Compounds2-Phenyl-2-propanol
Chemical structure of CAS 617-94-7

2-Phenyl-2-propanol

In Stock•Starting at $6 for 1 g•Purity ≥ 98%
CAS No.617-94-7
MDL No.N/A
MFC9H12O
MW136.19
InChI KeyBDCFWIDZNLCTMF-UHFFFAOYSA-N
CUSTOM SYNTHESIS

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
1 g98%$6In Stock
5 g98%$8In Stock
10 g98%$10In Stock
25 g98%$20In Stock
100 g98%$70In Stock
500 g98%$268In Stock
5 kg98%$2083In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

2-Phenylpropan-2-ol is a tertiary alcohol formed by replacing the hydrogen on the hydroxy-bearing carbon of isopropanol with a phenyl group. It is a benzyl alcohol, a Mycoplasma genitalium metabolite, and a human xenobiotic metabolite, derived from a cumene hydride.

CAS No.617-94-7
Product Name2-Phenyl-2-propanol
IrritantIrritant
Acute ToxicAcute Toxic
Signal Word:Danger
HCode:H302-H315-H319-H311
PCode:P264-P264+P265-P270-P280-P301+P317-P302+P352-P305+P351+P338-P321-P330-P332+P317-P337+P317-P362+P364-P501-P262-P316-P361+P364-P405

Related Articles

Studies related to this compound and its mechanism of action

Cumene oxidation by cis-[RuIV(bpy)2(py)(O)]2+, revisited.

Inorganic chemistry • Vol. 43, Issue 4 • 2004
PMID: 14966998DOI: 10.1021/ic035298j

Generation and reactivity toward oxygen of carbon-centered radicals containing indane, indene, and fluorenyl moieties.

The Journal of organic chemistry • Vol. 68, Issue 8 • 2003
PMID: 12688791DOI: 10.1021/jo026666o

Separation and identification of DMPO adducts of oxygen-centered radicals formed from organic hydroperoxides by HPLC-ESR, ESI-MS and MS/MS.

Journal of the American Society for Mass Spectrometry • Vol. 14, Issue 8 • 2003
PMID: 12892910DOI: 10.1016/S1044-0305(03)00336-2

The yeast glutaredoxins are active as glutathione peroxidases.

The Journal of biological chemistry • Vol. 277, Issue 19 • 2002
PMID: 11875065DOI: 10.1074/jbc.M111686200

Documentation

Similar Products