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6-Isopropyl-4-methyl-2-p-tolyl-5,6-dihydro-4H-[1,3]selenazin-4-ol is a complex organic compound with a unique structure. It is characterized by a [1,3]selenazin-4-ol core, which is a type of selenium-containing heterocycle. The molecule features an isopropyl group at the 6-position, a methyl group at the 4-position, and a p-tolyl group (a phenyl group with a methyl substituent) at the 2-position. The compound is a dihydro derivative, indicating that it has two hydrogen atoms added across a double bond, and it exists in a 5,6-dihydro form, suggesting the presence of a double bond between these two carbons in the ring structure. This specific arrangement of functional groups and atoms gives the compound its distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

219307-86-5

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219307-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219307-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,3,0 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 219307-86:
(8*2)+(7*1)+(6*9)+(5*3)+(4*0)+(3*7)+(2*8)+(1*6)=135
135 % 10 = 5
So 219307-86-5 is a valid CAS Registry Number.

219307-86-5Downstream Products

219307-86-5Relevant academic research and scientific papers

Synthesis and characterization of novel 1,3-selenazine derivatives. BF3·Et2O-assisted reaction of primary selenoamides with α,β-unsaturated ketones

Koketsu, Mamoru,Senda, Takayuki,Yoshimura, Katsuhiro,Ishihara, Hideharu

, p. 453 - 456 (1999)

Reaction of primary selenoamides with α,β-unsaturated ketones in the presence of BF3·Et2O provided 5,6-dihydro-4H-1,3-selenazine derivatives in high yields. Among the 1,3-selenazine diastereomers bearing two asymmetric carbons at the

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