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115852-00-1

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115852-00-1 Usage

General Description

N-(2-(3-(benzyloxy)phenyl)-2-oxoethyl)acetamide is a chemical compound with the molecular formula C21H21NO3. It is a derivative of acetamide and contains a benzyl group attached to the oxygen atom of a phenyl group. N-(2-(3-(benzyloxy)phenyl)-2-oxoethyl)acetaMide is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various biologically active molecules. It is also a potential drug candidate for the treatment of various diseases, including cancer and neurological disorders. The presence of the benzyl and phenyl groups in the structure makes it an important target for further studies on its pharmacological properties and potential applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 115852-00-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,8,5 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115852-00:
(8*1)+(7*1)+(6*5)+(5*8)+(4*5)+(3*2)+(2*0)+(1*0)=111
111 % 10 = 1
So 115852-00-1 is a valid CAS Registry Number.

115852-00-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-oxo-2-(3-phenylmethoxyphenyl)ethyl]acetamide

1.2 Other means of identification

Product number -
Other names N-<2-(3-benzyloxyphenyl)-2-oxoethyl>acetamide

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:115852-00-1 SDS

115852-00-1Relevant articles and documents

A concise synthesis of a novel insulin-like growth factor i receptor (IGF-IR) inhibitor

Slade, Joel,Bajwa, Joginder,Liu, Hui,Parker, David,Vivelo, James,Chen, Guang-Pei,Calienni, John,Villhauer, Edwin,Prasad, Kapa,Repic, Oljan,Blacklock, Thomas J.

, p. 825 - 835 (2012/12/30)

An efficient synthesis of a potent insulin-like growth factor I receptor (IGF-IR) inhibitor AEW541 (1) is described. The key step in the synthesis is the cis-selective reductive animation of cyclobutanone, which sets up the desired 1,3-stereochemistry of the cyclobutane ring. The amino group thus generated is used as a handle to build the pyrrolopyrimidine ring. The final step resulting in 1 is accomplished by alkylation of in situ generated mesylate with azetidine.

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