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Phenol, 2,6-bis(1,1-dimethylethyl)-4-(1-pyrrolidinylmethyl)-, also known as 4-(1-pyrrolidinylmethyl)-2,6-bis(1,1-dimethylethyl)phenol, is a complex organic compound with the chemical formula C18H29NO. It is a derivative of phenol, featuring a pyrrolidinyl group attached to the 4-position and two tert-butyl groups at the 2 and 6 positions. Phenol, 2,6-bis(1,1-dimethylethyl)-4-(1-pyrrolidinylmethyl)- is characterized by its molecular weight of 273.43 g/mol and a melting point of approximately 70-72°C. It is a white crystalline solid and is soluble in organic solvents. This specific phenol derivative is not widely used in commercial applications but may be found in research settings or as an intermediate in the synthesis of other compounds. It is important to handle this chemical with care due to its potential toxicity and irritant properties.

794-54-7

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794-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 794-54-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 794-54:
(5*7)+(4*9)+(3*4)+(2*5)+(1*4)=97
97 % 10 = 7
So 794-54-7 is a valid CAS Registry Number.

794-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-(pyrrolidin-1-ylmethyl)phenol

1.2 Other means of identification

Product number -
Other names Phenol,2,6-bis(1,1-dimethylethyl)-4-(1-pyrrolidinylmethyl)

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:794-54-7 SDS

794-54-7Upstream product

794-54-7Downstream Products

794-54-7Relevant academic research and scientific papers

Method for treating multiple sclerosis

-

, (2008/06/13)

Provided is a method of treating multiple sclerosis employing certain phenol and benzamide compounds.

Method of treating inflammatory bowel disease

-

, (2008/06/13)

Provided is a method for treating inflammatory bowel disease in mammals utilizing certain phenol and benzamide compounds.

Method of treating type I diabetes

-

, (2008/06/13)

Provided is a method for treating Type I diabetes in mammals utilizing certain phenol and benzamide compounds.

Method for treating inflammation

-

, (2008/06/13)

Provided are methods of treating inflammation, arthritis and muscular dystrophy and preventing ischemia-induced cell damage employing certain phenol and benzamide compounds.

Chemical process

-

, (2008/06/13)

Novel bis(3',5'-mono or dihydrocarbyl-4'-hydroxybenzyl)-1,3-diketones are prepared by reacting a (3',5'-mono or dihydrocarbyl-4'-hydroxybenzyl)-1,3-diketone with an N,N-dihydrocarbyl-2,6-mono or dihydrocarbyl-4-aminomethylphenol and an alkyl halide in the presence of an alkaline earth metal halide. The products are useful as antioxidants.

Chemical process for preparing 1,3 diketones

-

, (2008/06/13)

Novel (3',5'-dihydrocarbyl-4'-hydroxybenzyl)-1,3-diketones are prepared by reacting an N,N-dihydrocarbyl-2,6-dihydrocarbyl-4-aminomethylphenol with a 1,3-diketone in the presence of a basic substance. The products are useful as antioxidants.

Chemical process for preparing 1,3-diketones

-

, (2008/06/13)

Novel (3',5'-dihydrocarbyl-4'-hydroxybenzyl)-1,3-diketones are prepared by reacting an N,N-dihydrocarbyl-2,6-dihydrocarbyl-4-aminomethylphenol with a 1,3-diketone and an alkyl halide in the presence of an alkali or an alkaline earth metal hydride. The products are useful as antioxidants.

Chemical process

-

, (2008/06/13)

Novel 2,4-dihydrocarbylspiro[5.5]undeca-1,4,8-trien-3-one compounds are prepared by reacting an N,N-dihydrocarbyl,2,6-dihydrocarbyl-4-aminomethylphenol with a conjugated diene and an alkyl halide in a liquid solvent medium.

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