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1-Cyclohexen-1-amine, N-ethyl- is an organic compound with the chemical formula C8H15N. It is a derivative of cyclohexene, a cyclic hydrocarbon, with an amine group attached to the nitrogen atom. 1-Cyclohexen-1-amine, N-ethyl- is characterized by its six-membered carbon ring structure, with one double bond in the ring, and an ethylamine group (N-ethyl) attached to the nitrogen atom. It is a colorless liquid with a pungent odor and is soluble in water and organic solvents. 1-Cyclohexen-1-amine, N-ethyl- has potential applications in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. However, it is important to handle 1-Cyclohexen-1-amine, N-ethyl- with care, as it may have potential health hazards and should be stored and used according to proper safety guidelines.

103-68-4

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103-68-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103-68-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103-68:
(5*1)+(4*0)+(3*3)+(2*6)+(1*8)=34
34 % 10 = 4
So 103-68-4 is a valid CAS Registry Number.

103-68-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethylcyclohexen-1-amine

1.2 Other means of identification

Product number -
Other names CYCLOHEXENYL ETHYL AMINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:103-68-4 SDS

103-68-4Relevant academic research and scientific papers

Concise synthesis of the tricyclic skeleton of cylindricines using a radical cascade involving 6-endo selective cyclization

Taniguchi, Tsuyoshi,Tamura, Osamu,Uchiyama, Masahiko,Muraoka, Osamu,Tanabe, Genzoh,Ishibashi, Hiroyuki

, p. 1179 - 1181 (2005)

On treatment with Bu3SnH and azobis(cyclohexanecarbonitrile) (ACN), enamide 19 underwent a 6-endo-trig/5-endo-trig radical cascade to afford perhydropyrrolo[2,1-j]quinoline derivative 21, a cylindricine skeleton.

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