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6555-59-5

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6555-59-5 Usage

General Description

1-(1-methylcyclohex-3-en-1-yl)ethanone is a chemical compound with the molecular formula C10H16O. It is also known as pulegone and is commonly found in essential oils such as pennyroyal and Corsican mint. Pulegone has a minty odor and is used in the fragrance and flavor industries. It is also used as a mosquito repellent and has some medicinal properties, including potential use in the treatment of respiratory disorders and pain relief. Pulegone has been found to have toxic effects on the liver and is considered to be a potentially harmful chemical if ingested in large amounts.

Check Digit Verification of cas no

The CAS Registry Mumber 6555-59-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6555-59:
(6*6)+(5*5)+(4*5)+(3*5)+(2*5)+(1*9)=115
115 % 10 = 5
So 6555-59-5 is a valid CAS Registry Number.

6555-59-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-methylcyclohex-3-en-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-Acetyl-1-methylcyclohexen-3

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:6555-59-5 SDS

6555-59-5Relevant articles and documents

Anionic Oxy-Claisen Rearrangement of a Tricyclic α-Allyloxy Ketone

Kirchner, James J.,Pratt, Daniel V.,Hopkins, Paul B.

, p. 4229 - 4232 (2007/10/02)

Preparatively useful reaction conditions for the anionic oxy-Claisen rearrangement of an α-allyloxy ketone (6) possessing acidic α- and α'-hydrogens are described.The reaction rate and efficiency are strongly influenced by both solvent and counterion.The

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