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Zhengzhou Delong Chemical Co.
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當前位置:Zhengzhou Delong Chemical Co., Ltd.>>Fungicide>> Fungicide Boscalid CAS NO 188425-85-6

Fungicide Boscalid CAS NO 188425-85-6

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Zhengzhou Delong Chemical Co., Ltd.

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  • 商鋪產(chǎn)品:465條
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  • 注冊時間:2024-09-15
  • 最近登錄:2024-09-15
  • 聯(lián)系人:Technology Zone(East), Zhengzhou , Henan, China
產(chǎn)品簡介

Boscalid is a new nicotinamide fungicide developed by BASF company, Germany. It is mainly used to control powdery mildew, Botrytis Cinerea, various rot, brown rot and Root Rot. Pyridamide, a succinate-coq reductase inhibitor in the mitochondrial chain, has strong inhibition of Spore Germination and no cross-resistance to other fungicides.

詳情介紹

Product introduction

Product name: Boscalid

Chemical Formula: C18H12Cl2N2O

CAS NO: 188425-85-6

Appearance: White powder

Molecular Weight: 343.21

Structural Formula:

啶酰菌胺分子式


Toxicity: Acute transoral:  Gt; 2000mg / kg; acute transdermal:  Gt; 2000mg / kg, low toxicity bactericid

Storage: Store in a cool place. Keep container tightly closed and store in dry and ventilated place


Application

1.Boscalid is a broad-spectrum, systemic fungicide, it is effective in preventing and curing diseases resistant to sterol inhibitors, Bisimides, 1H-benzimidazole, pyrimidines, phenylamides, and methoxyacrylates. The product can be transported from the xylem to the top of the leaf tip and leaf margin of the plant Chemical book; it also has vertical Osmosis, which can be carried through the leaf tissue to the back of foliage's leaf; however, the product has very little redistribution in the vapor phase.  


2.Boscalid was mainly sprayed through stem and leaf, the dosage was 100 ~ 1,200 ga. I. / HM2

Boscalid is used to control powdery mildew, Mycosphaerella aspp on grapes, lawns, fruit trees, vegetables and ornamental plants, and diseases caused by altchical fungus Booker Nariaspp, botisspp and Sclerotinia Sclerotiorum. The compound preparation is also used on cble crops such as grains, grapes, peanuts and potatoes.


the application of Boscalid_副本


Synthetic method

1.Using o-chloronitrobenzene as raw material, Suziki reaction with P-CHLOROBENZOIC boric acid was firstly carried out, then reduced, and then condensed with 2-chloronicotinyl chloride to obtain the target product.


2.Using o-iodoaniline as raw material, the product was firstly reacted with 2-chloronicotinyl chloride and then Suzuki reaction with p-chlorophenylboric acid.

 

Package:25Kg/drum

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