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1,3-Butanedione, 4,4,4-trichloro-1-phenyl-, also known as chloral phenylhydrazone or trichlorophenylhydrazone, is a chemical compound with the molecular formula C10H8Cl3O2. It is a derivative of 1,3-butanedione (diacetyl), where one of the hydrogen atoms is replaced by a phenyl group, and three chlorine atoms are attached to the phenyl ring. 1,3-Butanedione, 4,4,4-trichloro-1-phenyl- is a colorless to pale yellow crystalline solid with a pungent odor. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential health hazards, it is important to handle 1,3-Butanedione, 4,4,4-trichloro-1-phenyl- with proper safety measures and in accordance with relevant regulations.

717-10-2

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717-10-2 Usage

Physical state

Colorless, volatile liquid

Odor

Pungent

Uses

a. Production of polycarbonates
b. Production of polyurethanes
c. Production of isocyanates
d. Chemical intermediate in the synthesis of various organic compounds

Hazardous nature

Yes, requires careful handling and storage

Health risks

Potential exposure risks, depending on handling and storage conditions

Check Digit Verification of cas no

The CAS Registry Mumber 717-10-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 717-10:
(5*7)+(4*1)+(3*7)+(2*1)+(1*0)=62
62 % 10 = 2
So 717-10-2 is a valid CAS Registry Number.

717-10-2Downstream Products

717-10-2Relevant academic research and scientific papers

CONDENSATION OF NITRILES WITH METHYL KETONES AS A METHOD FOR THE SYNTHESIS OF β-AMINOVINYL KETONES

Sosnovskikh, V. Ya.,Ovsyannikov, I. S.

, p. 1801 - 1805 (2007/10/02)

The condensation of nitriles containing aromatic substituents and of trichloroacetonitrile with methyl ketones in the presence of (phenylethylamino)magnesium bromide leads to β-aminovinyl ketones.Acid hydrolysis of the β-aminovinyl ketones gave high yields of the corresponding β-diketones.

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