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75393-95-2

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75393-95-2 Usage

Molecular structure

Contains two tert-butyl groups, a methoxyphenyl group, and a piperidin-1-ylmethyl group attached to a phenolic ring

Use

Commonly used in medicinal chemistry and pharmaceuticals

Pharmacological activities

Potential antioxidant, anti-inflammatory, and neuroprotective properties

Value

Valuable compound for further research and potential drug development

Check Digit Verification of cas no

The CAS Registry Mumber 75393-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,9 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75393-95:
(7*7)+(6*5)+(5*3)+(4*9)+(3*3)+(2*9)+(1*5)=162
162 % 10 = 2
So 75393-95-2 is a valid CAS Registry Number.

75393-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-[(4-methoxyphenyl)-piperidin-1-ylmethyl]phenol

1.2 Other means of identification

Product number -
Other names -

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:75393-95-2 SDS

75393-95-2Relevant articles and documents

Solvent-free microwave synthesis 4 - phenyl methylene - 2, 6 - di-tert-butyl - 2, 5 - cyclohexadiene -1 - ketone (by machine translation)

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Paragraph 0021-0023, (2019/04/30)

The invention discloses a 4 - benzylidene - 2, 6 - di-tert-butyl - 2, 5 - cyclohexadiene - 1 - ketone derivative (P -QM) green preparation method. Under the condition of using solvent-free microwave radiation heating, 2, 6 - di-tert-butyl phenol and aldehyde, through the Mannich condensation and [...] two-step reaction, to obtain the 4 - benzylidene - 2, 6 - di-tert-butyl - 2, 5 - cyclohexadiene - 1 - ketone derivative (P -QM). This method has the raw material is cheap, the atom economy is high, fast reaction time, environment friendly, without the use of hazardous reagent and solvent, synthetic step is simple and convenient and the like, and the mild reaction conditions, substrate range wide applicability, simple and safe operation, and is suitable for industrial production. (by machine translation)

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