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5-Chloro-benzofuran-3-one oxime is a chemical compound with the molecular formula C8H4ClNO2. It is a derivative of benzofuran-3-one, featuring a chloro substituent at the 5th position and an oxime group attached to the 3rd position. 5-chloro-benzofuran-3-one oxime is characterized by its aromatic structure, with the benzene ring fused to a furan ring, and the presence of a carbonyl group. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural features. The oxime group in particular can participate in various chemical reactions, making it a versatile building block for organic synthesis. The compound's properties, such as its reactivity and potential applications, are influenced by the presence of the chlorine atom, which can affect its electronic and steric characteristics.

669-66-9

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669-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 669-66-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,6 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 669-66:
(5*6)+(4*6)+(3*9)+(2*6)+(1*6)=99
99 % 10 = 9
So 669-66-9 is a valid CAS Registry Number.

669-66-9Downstream Products

669-66-9Relevant academic research and scientific papers

Q.S.A.R. DE DERIVES DE DIHYDRO-2,3 BENZOFURANNAMINE-3 INHIBITEURS DE CROISSANCE VEGETALE

Turan-Zitouni, G.,Berge, G.,Noel-Artis, A. M.,Chevallet, P.,Fulcrand, P.,Castel, J.

, p. 643 - 656 (2007/10/02)

A series of N-(aminoacetyl)-2,3-dihydro-3-benzofurannamine were synthetized and tested by means of the growth inhibition technical using Lepidium Sativum L. root meristem.Simultaneous applications of Fujita-Ban, Hansch methods and molecular connectivity have shown the preponderant role of lipophilicity and of pKa determined experimentally.

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