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4-(2-methylpropoxy)-N-[2-(pyridin-4-yl)-1,3-benzoxazol-5-yl]benzamide is a complex organic compound with a molecular formula of C24H20N2O3. It is characterized by a benzamide structure, which includes a benzene ring attached to a carboxamide group. The compound features a 1,3-benzoxazole ring system, which is fused to a pyridine ring at the 2-position, indicating a significant degree of aromaticity and potential for π-π interactions. The 4-position of the benzamide is substituted with a 2-methylpropoxy group, which introduces a branched alkyl chain and may influence the compound's solubility and lipophilicity. This chemical structure suggests potential applications in medicinal chemistry, possibly as a precursor or intermediate in the synthesis of pharmaceuticals, given the presence of both aromatic and heterocyclic moieties that are common in drug molecules. However, without specific context or application, it's challenging to provide a detailed summary of its properties or uses.

6008-38-4

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6008-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6008-38-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6008-38:
(6*6)+(5*0)+(4*0)+(3*8)+(2*3)+(1*8)=74
74 % 10 = 4
So 6008-38-4 is a valid CAS Registry Number.

6008-38-4SDS

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 4-(2-methylpropoxy)-N-(2-pyridin-4-yl-1,3-benzoxazol-5-yl)benzamide

1.2 Other means of identification

Product number -
Other names 4-(2-methylpropoxy)-N-(2-pyridin-4-ylbenzooxazol-5-yl)benzamide

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:6008-38-4 SDS

6008-38-4Downstream Products

6008-38-4Relevant academic research and scientific papers

Enzymatic desymmetrization of prochiral 2,3-bis(acetoxymethyl)bicyclo [2.2.1]hepta-2,5-diene and 2,3-bis(hydroxymethyl)bicyclo[2.2.1]hepta-2,5- diene

Ranchoux, Magali,Brunel, Jean-Michel,Iacazio, Gilles,Buono, Gerard

, p. 581 - 587 (1998)

Enzymatic desymmetrization of the title compound 1 is reported using various commercially available lipases in hydrolysis and alcoholysis reactions or ester synthesis. In this area, lipase Amano AK (Pseudomonas sp.) proved to be the best lipase whatever the experimental conditions used. The monoacetate product 2 is indifferently obtained with more than 95% enantiomeric excess (ee) as the levorotatory enantiomer 2a or the dextrorotatory one 2b.

Photochemical isomerization of norbornadiene-containing polytriazoles obtained by click chemistry polyaddition

Miladi, Imen Abdelhedi,Mudraboyina, Bhanu Prakash,Oueslati, Ahmed,Drockenmuller, Eric,Romdhane, Hatem Ben

, p. 223 - 231 (2014/01/06)

Polyesters and polyethers containing norbornadiene (NBD) and 1,2,3-triazole units in the main chain are prepared by step growth polymerization of diester or diether NBD-based dialkynes with different aromatic diazides using copper-catalyzed azide-alkyne c

A Convenient Synthesis of 7-Substituted Norbornadienes

Luh, Tien-Yau,Lung, Ching Leung

, p. 57 - 58 (2007/10/02)

7-Substituted norbornadienes were conveniently synthesized from the adduct of nickelocene and dimethyl acetylenedicarboxylate

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