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Oxazole, 5-(chloromethyl)-4-methyl-2-[4-(trifluoromethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

317318-99-3

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317318-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 317318-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,7,3,1 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 317318-99:
(8*3)+(7*1)+(6*7)+(5*3)+(4*1)+(3*8)+(2*9)+(1*9)=143
143 % 10 = 3
So 317318-99-3 is a valid CAS Registry Number.

317318-99-3Relevant academic research and scientific papers

A highly regioselective preparation of 4-chloromethyl-5-methyl-2-aryl-1,3- oxazoles

Lee, George T.,Jiang, Xinglong,Vedananda,Prasad, Kapa,Repic, Oljan

, p. 1461 - 1464 (2004)

A facile highly regioselective process is described for the formation of 4-chloromethyl-1,3-oxazoles from 1,3-oxazole N-oxide/HCl salts. An explanation is presented for the high regioselectivity in deoxygenation-chlorination using POCl3 with HC

A new approach to the synthesis of 2-aryl-4-halomethyl-5-methyl-1,3- oxazoles by highly regioselective direct halogenation with NBS or NCS/MeCN

Yamane, Taihei,Mitsudera, Hiroyuki,Shundoh, Takatsugu

, p. 2825 - 2832 (2007/10/03)

A simple and efficient method for the synthesis of 2-aryl-4-bromomethyl-5- methyl-1,3-oxazoles 2 and 2-aryl-4-chloromethyl-5-methyl-1,3-oxazoles 3 is described. The reaction of 2-aryl-4,5-dimethyl-1,3-oxazoles 1 with N-bromosuccinimide and N-chlorosuccini

Novel selective small molecule agonists for peroxisome proliferator-activated receptor δ (PPARδ) - Synthesis and biological activity

Sznaidman, Marcos L.,Haffner, Curt D.,Maloney, Patrick R.,Fivush, Adam,Chao, Esther,Goreham, Donna,Sierra, Michael L.,LeGrumelec, Christelle,Xu, H. Eric,Montana, Valerie G.,Lambert, Millard H.,Willson, Timothy M.,Oliver Jr., William R.,Sternbach, Daniel D.

, p. 1517 - 1521 (2007/10/03)

We report the synthesis and biological activity of a new series of small molecule agonists of the human Peroxisome Proliferator-Activated Receptor δ (PPARδ). Several hits were identified from our original libraries containing lipophilic carboxylic acids. Optimization of these hits by structure-guided design led to 7k (GW501516) and 7l (GW0742), which shows an EC50 of 1.1 nM against PPARδ with 1000-fold selectivity over the other human subtypes.

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