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19936-64-2

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19936-64-2 Usage

Type

Synthetic organic compound

Primary uses

Fungicide and antifungal agent, commonly applied to fruits, vegetables, and ornamental plants to prevent the growth of mold, mildew, and other fungal diseases

Mechanism of action

Inhibits the biosynthesis of ergosterol in fungal cells, disrupting their cell membrane and ultimately leading to cell death

Systemic properties

Can be absorbed by the plant and distributed throughout its tissues, providing long-lasting protection against fungal infections

Environmental and health concerns

Potential impact on human health and the environment, leading to its regulation and restricted use in some countries.

Check Digit Verification of cas no

The CAS Registry Mumber 19936-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,3 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19936-64:
(7*1)+(6*9)+(5*9)+(4*3)+(3*6)+(2*6)+(1*4)=152
152 % 10 = 2
So 19936-64-2 is a valid CAS Registry Number.

19936-64-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-chloroanilino)methylidene]naphthalen-1-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19936-64-2 SDS

19936-64-2Downstream Products

19936-64-2Relevant articles and documents

Synthesis, Structure, and Catalytic Hydrogenation Activity of [NO]-Chelate Half-Sandwich Iridium Complexes with Schiff Base Ligands

Lv, Wen-Rui,Li, Rong-Jian,Liu, Zhen-Jiang,Jin, Yan,Yao, Zi-Jian

, p. 8181 - 8188 (2021/05/26)

A series of N,O-coordinate iridium(III) complexes with a half-sandwich motif bearing Schiff base ligands for catalytic hydrogenation of nitro and carbonyl substrates have been synthesized. All iridium complexes showed efficient catalytic activity for the hydrogenation of ketones, aldehydes, and nitro-containing compounds using clean H2 as reducing reagent. The iridium catalyst displayed the highest TON values of 960 and 950 in the hydrogenation of carbonyl and nitro substrates, respectively. Various types of substrates with different substituted groups afforded corresponding products in excellent yields. All N,O-coordinate iridium(III) complexes 1-4 were well characterized by IR, NMR, HRMS, and elemental analysis. The molecular structure of complex 1 was further characterized by single-crystal X-ray determination.

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