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Cyclohexanone, 2-(3-chloro-2-butenyl)-, also known as 3-chloro-2-butenyl cyclohexanone or chlorocamphor, is a chemical compound with the molecular formula C10H15ClO. It is a colorless to pale yellow liquid with a pungent odor, and it is soluble in organic solvents. Cyclohexanone, 2-(3-chloro-2-butenyl)- is primarily used as a synthetic intermediate in the production of various chemicals, including fragrances, pharmaceuticals, and agrochemicals. It is also used as a solvent and a reagent in chemical reactions. Due to its potential health and environmental hazards, it is important to handle Cyclohexanone, 2-(3-chloro-2-butenyl)- with care, following proper safety guidelines and regulations.

939-60-6

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939-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 939-60-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 939-60:
(5*9)+(4*3)+(3*9)+(2*6)+(1*0)=96
96 % 10 = 6
So 939-60-6 is a valid CAS Registry Number.

939-60-6Downstream Products

939-60-6Relevant academic research and scientific papers

SYNTHESIS OF UNSATURATED TERTIARY AMINES AND α-ALLYL SUBSTITUTED KETONES FROM AZOMETHINES USING METAL COMPLEX CATALYSTS

Ibragimov, A. G.,Minsker, D. L.,Morozov, A. B.,Galkin, E. M.,Dzhemilev, U. M.,Tolstikov, G. A.

, p. 140 - 144 (2007/10/02)

A method has been developed for the regioselective synthesis of unsaturated tertiary amines via the reaction of magnesium amides, derived from Schiff bases, with allylic electrophiles in the presence of Pd and Cu complexes.The reaction of ketimines which

Highly Regio- and Stereospecific Palladium-Catalyzed Allylation of Enolates Derived from Ketones

Negishi, Ei-ichi,Matsushita, Hajime,Chatterjee, Sugata,John, Robert A.

, p. 3188 - 3190 (2007/10/02)

The reaction of potassium enoxyborates, readily obtainable by treating potassium enolates with a trialkylborane, e.g., triethylborane, with allylic electrophiles such as allylic chlorides and acetates in the presence of a catalytic amount of a palladium-p

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