4397-16-4

Basic information

• Product Name: Benzenemethanol, 2-hydroxy-3-(1-methylethyl)-
• CAS NO: 4397-16-4
• Molecular Formula: C10H14O2
• Molecular Weight: 166.22
• Mol File: 4397-16-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 2-hydroxy-3-(1-methylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-hydroxy-3-(1-methylethyl)-(4397-16-4)
• EPA Substance Registry System: Benzenemethanol, 2-hydroxy-3-(1-methylethyl)-(4397-16-4)

Safety Data

• Hazardous Substances Data: 4397-16-4(Hazardous Substances Data)

Usage

Appearance

Colorless liquid

Odor

Characteristic pungent odor

Aliases

Cumene hydroperoxide

Main Use

Chemical intermediate in the production of acetone and phenol

Industrial Applications

Used as a radical initiator in propylene oxide manufacture

Laboratory Applications

Utilized as a reagent in organic synthesis

Health Hazards

Potential skin and eye irritation upon exposure

Respiratory Effects

May have harmful effects on the respiratory system

Upstream product

• 88-69-7 2-(1-methylethyl)phenol 
• 67372-96-7 3-isopropylsalicylaldehyde 
• 50-00-0 formaldehyd 

Downstream Products

• 214077-01-7 8-Isopropyl-2,2-dimethyl-4H-benzo[1,3]dioxine 
• 80865-61-8 (3-isopropyl-2-methoxyphenyl)methanol 
• 1433061-10-9 C₁₆H₂₈O₂Si 
• 1433061-70-1 C₁₅H₂₂O₄ 
• 1433061-40-5 C₂₁H₃₆O₄Si 
• 1433062-00-0 (2R)-ethyl 2-(2’-bromomethyl-6’-isopropylphenoxy)propanoate 

Relevant articles and documents

Deconjugative α-Alkylation of Cyclohexenecarboxaldehydes: An Access to Diverse Terpenoids

A general and efficient method for the deconjugative α-alkylation of α,β-unsaturated aldehydes promoted by a synergistic effect between tBuOK and NaH, which considerably increases the reaction rate under mild conditions, is reported. The β,γ-unsaturated aldehyde, resulting from the α-alkylation, is transformed in high yield into the corresponding allyl acetate via a lead(IV) acetate-mediated oxidative fragmentation. This strategy could be used for the construction of the carbon skeleton of a wide variety of alkyl or arylterpenoids.

PHOSPHONIC ACID DERIVATES AND THEIR USE AS P2Y12 RECEPTOR ANTAGONISTS

The invention relates to 2-phenyl-pyrimidine derivatives containing a phosphonic acid motif and their use as P2Y12 receptor antagonists in the treatment and/or prevention of peripheral vascular, of visceral-, hepatic- and renal-vascular, of cardiovascular and of cerebrovascular diseases or conditions associated with platelet aggregation, including thrombosis in humans and other mammals. (I).

A concise total synthesis of triptolide

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