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Cyclohexadieneacetyl chloride is an organic compound with the chemical formula C8H9ClO. It is a colorless to pale yellow liquid that is soluble in organic solvents. cyclohexadieneacetyl chloride is a derivative of cyclohexadiene, which is a six-membered ring with two double bonds, and acetyl chloride, a reactive acylating agent. Cyclohexadieneacetyl chloride is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and ability to form stable carbon-carbon bonds. It is also known for its potential use in the preparation of polymers and other specialty chemicals. The compound should be handled with care due to its potential irritant and toxic properties, and it is important to follow proper safety protocols during its use and storage.

3217-88-7

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3217-88-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3217-88-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,1 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3217-88:
(6*3)+(5*2)+(4*1)+(3*7)+(2*8)+(1*8)=77
77 % 10 = 7
So 3217-88-7 is a valid CAS Registry Number.

3217-88-7Relevant academic research and scientific papers

Cross-conjugated compounds: microwave spectrum and ring planarity of 3-methylene-1,4-cyclohexadiene

Hutter, Wolfgang,Bodenseh, Hans-Karl,Koch, Andreas

, p. 73 - 84 (1994)

The unstable 3-methylene-1,4-cyclohexadiene, an isomer of toluene, has been prepared from benzoic acid.The hydrocarbon can be handled quite easily in the solid state, and in the gas phase at low pressures.Rotational transitions have been measured from 12

Conversion of 1,4-Dihydrobenzoic Acids to Polyformylbenzenes under Vilsmeier Reaction Conditions

Raju, B.,Krishna Rao, G. S.

, p. 197 - 199 (2007/10/02)

1,4-Dihydrobenzoic acids 1a-e are converted by a one-pot reaction to benzene- mono-, di- and tricarboxaldehydes under Vilsmeier reaction conditions in yields ranging from 6 to 65percent.The same methodology also serves to give naphthalene-1,3-dicarboxaldehyde (2f) from 1,4-dihydro-1-naphthoic acid (1f) in 91percent yield.

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