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1-Propanamine, 2-methyl-N-[2-(2-propenyl)cyclohexylidene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137496-58-3

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137496-58-3 Usage

General Description

1-Propanamine, 2-methyl-N-[2-(2-propenyl)cyclohexylidene]-, also known as dicyclanil, is a chemical compound used as an insecticide and acaricide. It is commonly used in veterinary medicine to control parasites in livestock, especially in sheep and cattle. Dicyclanil works by disrupting the growth of insects and mites, preventing them from developing into adult stages and reproducing. It is considered to have low toxicity to mammals and is relatively safe for use in livestock when applied according to the manufacturer's instructions. Dicyclanil is often found in topical formulations such as pour-ons or sprays, and it provides long-lasting protection against parasites.

Check Digit Verification of cas no

The CAS Registry Mumber 137496-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,9 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 137496-58:
(8*1)+(7*3)+(6*7)+(5*4)+(4*9)+(3*6)+(2*5)+(1*8)=163
163 % 10 = 3
So 137496-58-3 is a valid CAS Registry Number.

137496-58-3Relevant academic research and scientific papers

Lewis Acid-Promoted 3-Aza-Cope Rearrangement of N-Alkyl-N-allylenamines

Cook, Gregory R.,Barta, Nancy S.,Stille, John R.

, p. 461 - 467 (2007/10/02)

The 3-aza-Cope rearrangement of the N-alkyl-N-allylenamines derived from isobutyraldehyde, which proceeds thermally at 250 deg C, has been accelerated by a variety of electrophilic reagents to give γ,δ-unsaturated imines.Protic acids, such as HCl (0.5 equ

Preparation and 3-Aza-Cope Rearrangement of N-Alkyl-N-allyl Enamines

Cook, Gregory R.,Stille, John R.

, p. 5578 - 5583 (2007/10/02)

The charge-accelerated rearrangement of N-allyl-N-isobutyl enamine substrates to γ,δ-unsaturated imine products and subsequent reduction to the corresponding N-alkyl δ,ε-unsaturated amines is reported.Several routes to the N-allyl-N-isobutyl enamine

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