521925-06-4

Basic information

• Product Name: Cyclohexanol, 2-chloro-1-methyl-4-(1-methylethenyl)-, (1S,2S,4R)-
• CAS NO: 521925-06-4
• Molecular Formula: C10H17ClO
• Molecular Weight: 188.697
• Mol File: 521925-06-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cyclohexanol, 2-chloro-1-methyl-4-(1-methylethenyl)-, (1S,2S,4R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanol, 2-chloro-1-methyl-4-(1-methylethenyl)-, (1S,2S,4R)-(521925-06-4)
• EPA Substance Registry System: Cyclohexanol, 2-chloro-1-methyl-4-(1-methylethenyl)-, (1S,2S,4R)-(521925-06-4)

Safety Data

• Hazardous Substances Data: 521925-06-4(Hazardous Substances Data)

Upstream product

• 5989-27-5 D-limonene 
• 5989-54-8 (-)-(S)-limonene 

Downstream Products

• 22972-51-6 (1S,4R)-p-mentha-2,8-dien-1-ol 

Relevant articles and documents

Preparation method of (1S, 4R)-1-methyl-4-(1-methylvinyl)-2-cyclohexene-1-ol

The invention relates to a preparation method of (1S, 4R)-1-methyl-4-(1-methylvinyl)-2-cyclohexene-1-ol, and belongs to the technical field of organic solvents. The preparation method comprises the following steps: reacting limonene with a halogenating reagent to obtain an intermediate shown in a formula (1), then reacting the intermediate shown in the formula (1) with a tertiary amine compound to obtain an intermediate shown in a formula (2), and finally carrying out a pyrolysis elimination reaction on the intermediate shown in the formula (2) to obtain (1S, 4R)-1-methyl-4-(1-methylvinyl)-2-cyclohexene-1-ol. The preparation method has the advantages of mild conditions, no need of an oxidation process of hydrogen peroxide with high preparation condition requirements and high safety risk, no need of an expensive catalyst, high yield, high product purity, simple steps, and suitableness for industrial production.

Isolation and identification of terpene chlorohydrins found in cold-pressed orange oil

Three terpene chlorohydrins found in cold-pressed orange oil were concentrated by silica adsorption chromatography and purified by preparative HPLC. Formation of these chlorohydrins was determined to be the result of a reaction of d-limonene, the major component of cold-pressed oil, with hypochlorous acid, found in chlorinated treatment water used in the oil recovery process. NMR analyses indicated that the major chlorohydrin present was the diequatorially substituted (1R,2R,4R)-2-chloro-8-p-menthen-1-ol (1). The other two compounds were the diaxial trans stereoisomer, (1S,2S,4R)-2-chloro-8-p-menthen-1-ol (2), and the dichlorohydrin, (1R,2R,4R)-2,9-dichloro-8-p-menthen-1-ol (3).