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5427-02-1

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5427-02-1 Usage

General Description

2,6-di-tert-butyl-4-(propan-2-ylidene)cyclohexa-2,5-dien-1-one is a chemical compound with the molecular formula C18H28O. It is a yellow crystalline solid that is primarily used as a fragrance ingredient in perfumes and personal care products. It is also used in the production of plastics and as a flavoring agent in the food industry. The compound is known for its strong and long-lasting scent, and it is often used in combination with other aromatic compounds to create unique and complex fragrance profiles. Although it has low acute toxicity, proper handling and storage of 2,6-di-tert-butyl-4-(propan-2-ylidene)cyclohexa-2,5-dien-1-one are necessary to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 5427-02-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5427-02:
(6*5)+(5*4)+(4*2)+(3*7)+(2*0)+(1*2)=81
81 % 10 = 1
So 5427-02-1 is a valid CAS Registry Number.

5427-02-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-propan-2-ylidenecyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2,6-Di-tert-butyl-4-isopropyliden-cyclohexa-2,5-dienon

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:5427-02-1 SDS

5427-02-1Relevant articles and documents

4,4′-(Trimethylene)bis(2,6-di-t-butylphenoxy) diradical: An application of the sequential redox-solid state photolysis (SRSSP) method

Nakatuji, Koji,Oda, Masaji,Kozaki, Masatoshi,Morimoto, Yoshiki,Okada, Keiji

, p. 845 - 846 (1998)

The oxidation of 4,4′-(trimethylene)bis(2,6-di-t-butylphenol) with lead dioxide underwent intramolecular cyclization at the 4,4′-positions to give a dispiro-compound. Irradiation of the dispiro-compound in a methylcyclohexane matrix at -150 °C produced 4,

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