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Phenol, 2,2'-methylenebis[4-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55252-54-5

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55252-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55252-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,5 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55252-54:
(7*5)+(6*5)+(5*2)+(4*5)+(3*2)+(2*5)+(1*4)=115
115 % 10 = 5
So 55252-54-5 is a valid CAS Registry Number.

55252-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethyl-2-[(5-ethyl-2-hydroxyphenyl)methyl]phenol

1.2 Other means of identification

Product number -
Other names Phenol,2,2'-methylenebis[4-ethyl

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:55252-54-5 SDS

55252-54-5Downstream Products

55252-54-5Relevant academic research and scientific papers

Development of chemical probes: Toward the mode of action of a methylene-linked di(aryl acetate) E1

Smith, Mark E.B.,Gunn, Richard M.,Rosivatz, Evelyn,Mak, Lok H.,Woscholski, Ruediger,Hailes, Helen C.

experimental part, p. 4917 - 4927 (2010/09/10)

Analogues of the novel inhibitor of the PI3-K/PKB pathway, 2-[5-(2-chloroethyl)-2-acetoxy-benzyl]-4-(2-chloroethyl)-phenyl acetate (E1), have been prepared and preliminary SAR performed. This established that at least one of the chloroethyl para-substituents could be removed or modified and the ability to inhibit PKB/Akt activation retained. Synthetic methodologies were then developed to methylene-linked aryl acetates for use as molecular probes to identify the target of compound E1.

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