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5-Hydroxy-p-mentha-1,4-dione, also known as pulegone, is a naturally occurring monoterpene ketone found in several plants, including pennyroyal, peppermint, and spearmint. It is an organic compound with the molecular formula C10H16O2 and has a molecular weight of 168.24 g/mol. Pulegone is characterized by its strong, minty aroma and is used in the fragrance and flavoring industries. It is also known for its potential medicinal properties, such as its ability to act as a bronchodilator and antispasmodic. However, it is important to note that pulegone can be toxic in high doses, leading to liver damage and other health issues, so it should be used with caution and in accordance with safety guidelines.

4586-59-8

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4586-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4586-59-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,8 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4586-59:
(6*4)+(5*5)+(4*8)+(3*6)+(2*5)+(1*9)=118
118 % 10 = 8
So 4586-59-8 is a valid CAS Registry Number.

4586-59-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-2-isopropyl-5-methyl-[1,4]benzoquinone

1.2 Other means of identification

Product number -
Other names 2-hydroxythymoquinone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4586-59-8 SDS

4586-59-8Relevant academic research and scientific papers

Synthesis, structural assignments and antiinfective activities of 3-O-benzyl-carvotacetone and 3-hydroxy-2-isopropyl-5-methyl-p-benzoquinone

Masila, Veronica M.,Ndakala, Albert J.,Byamukama, Robert,Midiwo, Jacob O.,Kamau, Rahab W.,Wang, Mei,Kumarihamy, Mallika,Zhao, Jianping,Heydreich, Matthias,Muhammad, Ilias

, p. 3599 - 3607 (2021)

In an attempt to synthesize carvotacetone analogues, new 3-O-benzyl-carvotacetone (10) and previously reported 3-hydroxy-2-isopropyl-5-methyl-p-benzoquinone (11) were synthesized from piperitone (7). In this work, we describe the synthesis of 10 and other

Total Synthesis of (?)-Perezoperezone through an Intermolecular [5+2] Homodimerization of Hydroxy p-Quinone

Long, Yang,Ding, Yiming,Wu, Hai,Qu, Chunlei,Liang, Hong,Zhang, Min,Zhao, Xiaoli,Long, Xianwen,Wang, Shu,Puno, Pema-Tenzin,Deng, Jun

, p. 17552 - 17557 (2019/11/16)

The first copper-catalyzed intermolecular [5+2] homodimerization of hydroxy p-quinone is presented, furnishing bicyclo[3.2.1]octadienone core structures in typically good yields and excellent diastereoselectivities. Applying this synthetic approach enables a concise nine-step total synthesis of (?)-perezoperezone from commercially available 3,5-dimethoxytoluene.

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