15804-78-1 Usage
Description
1-(2,4-DIMETHOXYPHENYL)-2-NITROPROPENE, with the molecular formula C11H13NO4, is a nitroalkene derivative of 2,4-DIMETHOXYPHENYL. It is a yellow liquid at room temperature and is highly reactive, making it a significant reagent in organic chemistry. This chemical compound serves as an important intermediate in the production of various organic compounds and is widely utilized in the synthesis of numerous bioactive molecules, including pharmaceuticals and other chemical products.
Uses
Used in Pharmaceutical Industry:
1-(2,4-DIMETHOXYPHENYL)-2-NITROPROPENE is used as a precursor in the synthesis of various pharmaceuticals for [application reason]. Its reactivity and versatility in organic synthesis make it a valuable component in the development of new drugs and medications.
Used in Chemical Products Industry:
1-(2,4-DIMETHOXYPHENYL)-2-NITROPROPENE is used as an intermediate in the production of a variety of chemical products for [application reason]. Its role in creating different organic compounds contributes to the diversity and functionality of chemical products available in the market.
Used in Organic Synthesis:
1-(2,4-DIMETHOXYPHENYL)-2-NITROPROPENE is used as a reagent in organic synthesis for [application reason]. Its high reactivity allows for the creation of a wide range of bioactive molecules, which can be further utilized in various applications, including the development of new pharmaceuticals and other chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 15804-78-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,0 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15804-78:
(7*1)+(6*5)+(5*8)+(4*0)+(3*4)+(2*7)+(1*8)=111
111 % 10 = 1
So 15804-78-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO4/c1-8(12(13)14)6-9-4-5-10(15-2)7-11(9)16-3/h4-7H,1-3H3/b8-6+
15804-78-1Relevant articles and documents
Binding of Phenylalkylamine Derivatives at 5-HT1C and 5-HT2 Serotonin Receptors: Evidence for a Lack of Selectivity
Glennon, Richard A.,Raghupathi, Reva,Bartyzel, Piotr,Teitler, Milt,Leonhardt, Sigrun
, p. 734 - 740 (2007/10/02)
Certain phenyalkylamine derivatives have been considered to bind selectively at 5-HT2 serotonin receptors.It is now recognized that the most widely used derivatives, i.e., 1-(2,5-dimethoxy-4-X-phenyl)-2-aminopropanes where X = Me (DOM), Br (DOB), and I (DOI) (1-3, respectively) also bind at the more recently identified population of serotonin 5-HT1C receptors.The purpose of the present investigation was to determine whether simple phenylalkylamines bind selectively at one population of receptors over the other.An examination of 34 derivatives reveals (i) similar structure-affinity relationships and (ii) a significant correlation (r = >0.9, n = 25) between 5-HT1C and 5-HT2 affinity.None of the compounds included in the present study displayed more than a 10-fold selectivity for one population of these receptors over the other; the results suggest that these compounds (including the widely used 5-HT2 agonists DOB and DOI) are 5-HT1C/5-HT2 agents.
A Simple Unusual One-Step Conversion of Aromatic Aldehydes into Nitriles
Karmarkar, Sanjay N.,Kelkar, Shriniwas L.,Wadia, Murzban S.
, p. 510 - 512 (2007/10/02)
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