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2-Oxazolidinone, 4-(phenylmethyl)-3-[(2,2,2-trifluoroethoxy)acetyl]-, (4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

177785-24-9

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177785-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177785-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,7,8 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 177785-24:
(8*1)+(7*7)+(6*7)+(5*7)+(4*8)+(3*5)+(2*2)+(1*4)=189
189 % 10 = 9
So 177785-24-9 is a valid CAS Registry Number.

177785-24-9Downstream Products

177785-24-9Relevant academic research and scientific papers

Use of an antagonist of PPAR alpha and PPAR gamma for the treatment of syndrome X

-

, (2008/06/13)

PCT No. PCT/EP97/00058 Sec. 371 Date Sep. 10, 1998 Sec. 102(e) Date Sep. 10, 1998 PCT Filed Jan. 7, 1997 PCT Pub. No. WO97/25042 PCT Pub. Date Jul. 17, 1997A method for the treatment or prophylaxis of Syndrome X in a human or non-human mammal is disclosed. The method comprises the administration of an effective, non-toxic and pharmaceutically effective amount of an agonist of PPAR alpha and PPAR gamma , or a pharmaceutically acceptable derivative thereof, to a human or non-human mammal in need thereof.

Non-thiazolidinedione antihyperglycaemic agents. Part 5: Asymmetric aldol synthesis of (S)-(-)-2-oxy-3-arylpropanoic acids

Haigh, David,Birrell, Helen C.,Cantello, Barrie C. C.,Eggleston, Drake S.,Haltiwanger, R. Curtis,Hindley, Richard M.,Ramaswamy, Anantha,Stevens, Nicola C.

, p. 1353 - 1367 (2007/10/03)

Boron-mediated asymmetric aldol reactions of substituted benzaldehyde 5 with 2-oxyethanoyloxazolidinones 4a-e, containing electron withdrawing, chelating, and bulky alkoxy and aryloxy groups, gave variable yields of syn- aldol adducts 6a-e in high diastereoisomeric excess. Dehydroxylation of these adducts afforded 7a-e in a sequence which complements the traditional Evans asymmetric alkylation strategy. Cleavage of the auxiliary from 7a-e afforded antihyperglycaemic (S)-(-)-2-oxy-3-arylpropanoic acids 3a-e in excellent enantiomeric excess.

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