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(Z)-2-Phenyl-2-butenoyl chloride, also known as cinnamoyl chloride or 3-phenylpropenoyl chloride, is an organic compound with the chemical formula C10H9ClO. It is a colorless to pale yellow liquid with a pungent odor and is derived from the reaction of cinnamic acid with thionyl chloride or phosphorus pentachloride. This chemical is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds, such as cinnamic acid derivatives, which are used as flavoring agents and fragrances. It is also utilized in the preparation of polymers and resins. Due to its reactivity, it is essential to handle (Z)-2-Phenyl-2-butenoyl chloride with caution, as it can cause irritation to the eyes, skin, and respiratory system, and may be harmful if ingested or inhaled.

60995-95-1

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60995-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60995-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,9 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60995-95:
(7*6)+(6*0)+(5*9)+(4*9)+(3*5)+(2*9)+(1*5)=161
161 % 10 = 1
So 60995-95-1 is a valid CAS Registry Number.

60995-95-1Upstream product

60995-95-1Downstream Products

60995-95-1Relevant academic research and scientific papers

Electrochemical oxidative: Z -selective C(sp2)-H chlorination of acrylamides

Coles, Simon J.,Hareram, Mishra Deepak,Harnedy, James,Morrill, Louis C.,Tizzard, Graham J.

supporting information, p. 12643 - 12646 (2021/12/07)

An electrochemical method for the oxidative Z-selective C(sp2)-H chlorination of acrylamides has been developed. This catalyst and organic oxidant free method is applicable across various substituted tertiary acrylamides, and provides access to a broad range of synthetically useful Z-β-chloroacrylamides in good yields (22 examples, 73% average yield). The orthogonal derivatization of the products was demonstrated through chemoselective transformations and the electrochemical process was performed on gram scale in flow.

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