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6-(1-hydroxy-1-methylethyl)-3-methyl-2-cyclohexen-1-ol, also known as cis-isopulegol, is a naturally occurring organic compound found in essential oils, particularly in the oils of basil and other mints. It is a monoterpene alcohol with a molecular formula of C10H18O2 and a molecular weight of 170.25 g/mol. 6-(1-hydroxy-1-methylethyl)-3-methyl-2-cyclohexen-1-ol has a unique structure, featuring a cyclohexene ring with a hydroxyl group, a methyl group, and an isopropyl group attached to it. Cis-isopulegol is known for its potential applications in the synthesis of menthol and other valuable compounds, as well as its use as a fragrance ingredient. It is also being studied for its potential therapeutic properties, such as its ability to inhibit acetylcholinesterase, an enzyme involved in the breakdown of the neurotransmitter acetylcholine.

6252-34-2

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6252-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6252-34-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6252-34:
(6*6)+(5*2)+(4*5)+(3*2)+(2*3)+(1*4)=82
82 % 10 = 2
So 6252-34-2 is a valid CAS Registry Number.

6252-34-2Relevant academic research and scientific papers

PROCESS AND COMPOUNDS FOR PREPARATION OF CANNABINOIDS

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Paragraph 0057; 0062-0063, (2020/06/05)

The invention involves condensation of various derivatives of cyclic alkene alcohols of Formula (II) or Formula (III) where, R1 is alkyl, aryl, alkyl aryl or heterocyclic carbamoyl. R2 is either R1 as mentioned earlier or an acyl group, -C(=O)-R3 where, R3 is selected from a group comprising (subst)C1-C12 alkyl, (subst)aryl, alkyl aryl with olivetol to get (-)-trans-?9-tetrahydrocannabinol (also known as Dronabinol, Formula (I)). The process disclosed provides high purity of dronabinol at crude stage making it easy for purification.

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

Arbuzov, B. A.,Isaeva, Z. G.,Belyaeva, M. G.,Ratner, V. V.,Kataeva, O. N.,et al.

, p. 117 - 119 (2007/10/02)

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.

Total Synthesis of (+)-Balanitol and of (+)-Selin-4-(15)-ene-1β,11-diol

Anglea, Timothy A.,Pinder, A. Reginald

, p. 5537 - 5544 (2007/10/02)

(+)-Balanitol (1) and (+)-selin-4-(15)-ene-1β,11-diol (2), two recently isolated naturally occurring eudesmanoid bicyclic sesquiterpene alcohols, have been synthesized stereoselectively by a route involving a photocycloaddition of a cyclobutene and

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