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(E)-3-Cyclohexyl-2-propenylamin is an organic compound with the molecular formula C9H17N. It is a derivative of cyclohexene, featuring a cyclohexyl group attached to a 2-propenylamine chain. (E)-3-Cyclohexyl-2-propenylamin is characterized by its aliphatic amine structure, with a double bond between the second and third carbon atoms, indicating the (E)-configuration. It is a colorless to pale yellow liquid with a strong amine-like odor. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is important to handle (E)-3-Cyclohexyl-2-propenylamin with care, following appropriate safety measures to prevent potential health and environmental risks.

4441-52-5

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4441-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4441-52-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4441-52:
(6*4)+(5*4)+(4*4)+(3*1)+(2*5)+(1*2)=75
75 % 10 = 5
So 4441-52-5 is a valid CAS Registry Number.

4441-52-5Relevant academic research and scientific papers

A catalytic asymmetric chlorocyclization of unsaturated amides

Jaganathan, Arvind,Garzan, Atefeh,Whitehead, Daniel C.,Staples, Richard J.,Borhan, Babak

, p. 2593 - 2596 (2011/05/02)

The asymmetric chlorocyclization of unsaturated amides catalyzed by (DHQD)2PHAL yields oxazoline and dihydrooxazine derivatives (see scheme). The reaction is operationally simple and employs 1-2 mol % of the commercially available (DHQD)2PHAL (hydroquinidine 1,4-phthalazinediyl diether) catalyst. Different substitution patterns of the olefin as well as aromatic and aliphatic olefin substituents are well tolerated. DCDPH=N,N-dichloro-5,5-diphenylhydantoin. Copyright

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