57030-53-2

Basic information

• Product Name: 4-hydroxy-alpha,alpha,4-trimethylcyclohex-2-ene-1-methanol
• Synonyms: 4-hydroxy-alpha,alpha,4-trimethylcyclohex-2-ene-1-methanol;2-(4-Methyl-4-hydroxy-2-cyclohexenyl)-2-propanol;4-Hydroxy-α,α,4-trimethyl-2-cyclohexene-1-methanol;p-Mentha-2-ene-1,8-diol
• CAS NO: 57030-53-2
• Molecular Formula: C₁₀H₁₈O₂
• Molecular Weight: 170.24872
• EINECS: 260-524-2
• Mol File: 57030-53-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 268°Cat760mmHg
• Flash Point: 122°C
• Appearance: /
• Density: 1.048g/cm³
• Vapor Pressure: 0.00106mmHg at 25°C
• Refractive Index: 1.51
• CAS DataBase Reference: 4-hydroxy-alpha,alpha,4-trimethylcyclohex-2-ene-1-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxy-alpha,alpha,4-trimethylcyclohex-2-ene-1-methanol(57030-53-2)
• EPA Substance Registry System: 4-hydroxy-alpha,alpha,4-trimethylcyclohex-2-ene-1-methanol(57030-53-2)

Safety Data

• Hazardous Substances Data: 57030-53-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H18O2/c1-9(2,11)8-4-6-10(3,12)7-5-8/h4,6,8,11-12H,5,7H2,1-3H3

Upstream product

• 54145-81-2 1,2-epoxy-8-hydroxy-p-menthane 
• 98-55-5 terpineol 
• 76338-34-6 1α-hydroxy-2β-phenylseleno-trans-p-menthan-8-ol 
• 554-61-0 2-carene 

Downstream Products

• 87791-00-2 6-(1-hydroxy-1-methylethyl)-3-methyl-2-cyclohexen-1-one 
• 76338-37-9 1,8-diacetoxy-trans-p-menth-2-ene 

Relevant articles and documents

ELECTROPHILIC ADDITION OF LEAD TETRAACETATE TO 2-CARENE IN AN ACIDIDIC MEDIUM

Oxidation of 2-carene by lead tetraacetate in acetic acid afforded p-menth-1(10),2-dien-7-ol, 2-acetyl-6,6-dimethylbicyclohexane, p-menth-2-ene-1α,7-diol, p-menth-1-ene-3β,7-diol, and 2-(m-tolyl)propanol-2.Keywords: oxidation, lead tetraacetate, 2-carene, benzene, acetic acid, medium polarity.

Studies on the stereochemical course of selenium-assisted cyclisation: Biogenetic-type synthesis in the p-menthan series

Acid-catalysed cyclisation of the β-hydroxy selenide (3) denved from linalyl acetate (1) afforded the trans-p-methans (4) and (5), the structures of which were confirmed by their transformation into (6), (8), (9), and (11) and by alternative synthesis of these compounds.