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(-)-(1S,2R,3S,4aR,5S,8S,8aS)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-ethynyl-3,8-dimethyl-5-triisopropylsilanyloxy-decahydro-naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1187676-85-2

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1187676-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1187676-85-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,7,6,7 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1187676-85:
(9*1)+(8*1)+(7*8)+(6*7)+(5*6)+(4*7)+(3*6)+(2*8)+(1*5)=212
212 % 10 = 2
So 1187676-85-2 is a valid CAS Registry Number.

1187676-85-2Relevant academic research and scientific papers

NOVEL MK8383 ANALOGUE AND DISEASE CONTROL AGENT FOR AGRICULTURAL OR HORTICULTURAL PURPOSES

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Page/Page column 25, (2010/12/30)

An objective of the present invention is to provide agricultural and horticultural disease control agents that have potent control effect against plant diseases and, at the same time, have high photostability. The agricultural and horticultural disease control agents comprise a novel substance analogous to MK8383 as an active ingredient.

Synthesis of NH006 - A photostable fungicide effective against Botrytis cinerea - According to the asymmetric total synthesis of MK8383

Hayashi, Nobuyuki,Yamamoto, Kentaro,Minowa, Nobuto,Mitomi, Masaaki,Nakada, Masahisa

supporting information; experimental part, p. 1821 - 1825 (2010/08/21)

MK8383, isolated from Phoma sp. T2526 in 1993, exhibits potent antibiotic activities against a variety of phytopathogens and has been considered a promising fungicide against Botrytis cinerea. Unfortunately, MK8383 is a photosensitive compound and it undergoes irreversible decomposition. Although much effort has been devoted to improving the photostability of MK8383 by chemical modification of its structure by a research group organized by Meiji Seika Kaishya, Ltd. and Mitsubishi Chemical Corporation, a photostable MK8383 derivative has never been prepared. We have found that a C13-14 double bond of MK8383 and (+)-phomopsidin is responsible for the photosensitivity, and herein, we report the synthesis of NH006, an MK8383 derivative with a saturated C13-14 double bond and (S) configuration at C14, based on the asymmetric total synthesis of MK8383. NH006 exhibits good photostability and potent antifungal activity against B. cinerea.

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