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Benzaldehyde, 2,6-dimethyl-3,5-dinitro-, also known as 2,6-dimethyl-3,5-dinitrobenzaldehyde, is an organic compound with the chemical formula C9H8N2O4. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. Benzaldehyde, 2,6-dimethyl-3,5-dinitro- is characterized by the presence of a benzaldehyde functional group, with two methyl groups at the 2nd and 6th carbon positions, and two nitro groups at the 3rd and 5th carbon positions. It is synthesized through various chemical reactions and is used in the production of dyes, pharmaceuticals, and other organic compounds. Due to its reactivity and potential applications, it is an important intermediate in organic synthesis.

111159-80-9

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111159-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111159-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,5 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 111159-80:
(8*1)+(7*1)+(6*1)+(5*1)+(4*5)+(3*9)+(2*8)+(1*0)=89
89 % 10 = 9
So 111159-80-9 is a valid CAS Registry Number.

111159-80-9Upstream product

111159-80-9Relevant academic research and scientific papers

Potential antisecretory antidiarrheals. 1. α2-Adrenergic aromatic aminoguanidine hydrazones

Pitzele,Moormann,Gullikson,Albin,Bianchi,Palicharla,Sanguinetti,Walters

, p. 138 - 144 (1988)

Guanabenz, a centrally acting antihypertensive agent, has been shown to have intestinal antisecretory properties. A series of aromatic aminoguanidine hydrazones was made in an effort to separate the antisecretory and cardiovascular activities. Benzaldehyde, naphthaldehyde, and tetralone derivatives were synthesized. The compounds were evaluated in the cholera toxin treated ligated jejunum of the rat and in the Ussing chamber using a rabbit ileum preparation. A number of compounds, including members of each structural class, were active upon subcutaneous administration in the rat. Active compounds were determined to be α2-adrenergic agonists by yohimbine reversals of their Ussing chamber activities. The compound displaying the best separation of activities was the aminoguanidine hydrazone of 2,6-dimethyl-4-hydroxybenzaldehyde (20).

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