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ethyl (2E,4E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-(trifluoromethyl)penta-2,4-dienoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1403369-91-4

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1403369-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403369-91-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,3,6 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1403369-91:
(9*1)+(8*4)+(7*0)+(6*3)+(5*3)+(4*6)+(3*9)+(2*9)+(1*1)=144
144 % 10 = 4
So 1403369-91-4 is a valid CAS Registry Number.

1403369-91-4Downstream Products

1403369-91-4Relevant academic research and scientific papers

Insights into the in Vitro and in Vivo SAR of Abscisic Acid – Exploring Unprecedented Variations of the Side Chain via Cross-Coupling-Mediated Syntheses

Frackenpohl, Jens,Grill, Erwin,Bojack, Guido,Baltz, Rachel,Busch, Marco,Dittgen, Jan,Franke, Jana,Freigang, J?rg,Gonzalez, Susana,Heinemann, Ines,Helmke, Hendrik,Hills, Martin,Hohmann, Sabine,von Koskull-D?ring, Pascal,Kleemann, Jochen,Lange, Gudrun,Lehr, Stefan,Müller, Thomas,Peschel, Elisabeth,Poree, Fabien,Schmutzler, Dirk,Schulz, Arno,Willms, Lothar,Wunschel, Christian

, p. 1403 - 1415 (2018/04/06)

Novel analogues of the plant hormone abscisic acid (ABA) were designed and prepared to explore the impact that modifications of its terpenoid side chain have on receptor affinity and in vivo efficacy against drought stress in selected crops. Their efficient and versatile synthesis proceeded via Stille or Sonogashira couplings, shortening the synthetic route significantly. In line with molecular modelling and X-ray crystallography studies novel ABA-derivatives with small alkyl, cycloalkyl or haloalkyl substituents showed strong effects in vitro and in vivo against drought stress in crops, particularly canola and wheat.

SUBSTITUTED 5-(CYCLOHEX-2-EN-1-YL)-PENTA-2,4-DIENES AND 5-(CYCLOHEX-2-EN-1-YL)-PENT-2-EN-4-INES AS ACTIVE AGENTS AGAINST ABIOTIC STRESS IN PLANTS

-

, (2014/04/03)

The invention relates to substituted 5-(cyclohex-2-en-1-yl)penta-2,4-dienes and 5-(cyclohex-2-en-1-yl)pent-2-en-4-ines of the formula (I) and their salts where the radicals R1, R2, R3, R4, [X—Y] and Q are each as defined in the description, to processes for preparation thereof and to the use thereof for enhancing stress tolerance in plants with respect to abiotic stress, and/or for increasing plant yield.

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