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2,2,4-Trimethyl-5-phenyl-2,3,4,5-tetrahydroisoxazole is a complex organic compound with the molecular formula C14H19NO. It is a derivative of isoxazole, a heterocyclic compound containing a five-membered ring with one oxygen and one nitrogen atom. The structure of 2,2,4-trimethyl-5-phenyl-2,3,4,5-tetrahydroisoxazole is characterized by a tetrahydroisoxazole ring, which is a reduced form of isoxazole, and a phenyl group attached to the 5-position. The molecule also contains three methyl groups, two of which are located at the 2-position and one at the 4-position. 2,2,4-trimethyl-5-phenyl-2,3,4,5-tetrahydroisoxazole of is interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other chemical products due to its unique structure and properties.

60980-85-0

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60980-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60980-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,8 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60980-85:
(7*6)+(6*0)+(5*9)+(4*8)+(3*0)+(2*8)+(1*5)=140
140 % 10 = 0
So 60980-85-0 is a valid CAS Registry Number.

60980-85-0Upstream product

60980-85-0Relevant academic research and scientific papers

Reductive Alkylation of β-Alkanolamines with Carbonyl Compounds and Sodium Borohydride

Saavedra, Joseph E.

, p. 2271 - 2273 (2007/10/02)

A synthesis of secondary alkylalkanolamines from primary alkanolamines in a rapid process in which overalkylation is virtually suppressed is described.The procedure combines the ease of formation of oxazolidines from alkanolamines with aldehydes or ketones in absolute ethanol and the lability of the newly formed C-O bond toward sodium borohydrode.The entire process is carried out in 15-35 min depending on the carbonyl substrate.