18917-76-5

Usage

Natural occurrence

Grapefruit

Synthetic availability

Can be synthesized in a lab

Uses

Flavor and fragrance additive in perfumes, colognes, and food items

Aroma

Citrusy, woody

Insect-repelling properties

Commonly used in insect repellents and pesticides

Potential medical applications

Anti-inflammatory and anti-cancer agent (under study)

InChI:InChI=1/C11H13NO4/c1-8(12(13)14)4-9-5-10(15-2)7-11(6-9)16-3/h4-7H,1-3H3

Upstream product

• 79-24-3 Nitroethane 
• 7311-34-4 3,5-dimethoxybenzaldehdye 

Downstream Products

• 15402-82-1 1-(3,5-dimethoxyphenyl)propan-2-amine 
• 126760-79-0 3-(3,5-Dimethoxy-phenyl)-4-methyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 18917-77-6 (3,5-dimethoxyphenyl)acetone 
• 1215288-80-4 1-acetylamino-2-bromo-1-(3,5-dimethoxyphenyl)-2-nitropropane 
• 126760-88-1 (5Z,10Z,14Z,19Z)-2,7,12,17-Tetrakis-(3,5-dimethoxy-phenyl)-3,8,13,18-tetramethyl-porphyrin 
• 183256-23-7 (R)-N-<1-(3,5-dimethoxyphenyl)-2-propylidene>-α-methylbenzenemethanamine 
• 250212-49-8 (R,R)-N-<1-(3,5-dimethoxyphenyl)-2-propyl>-α-methylbenzenemethanamine 

Relevant academic research and scientific papers

Synthesis of carbocyclic analogs of dehydroaltenusin: Identification of a stable inhibitor of calf DNA polymerase α

Syntheses of carbocyclic analogs of dehydroaltenusin tautomers are reported. Both target compounds, cDHA (2,8-dihydroxy-6-methoxy-10a-methyl-10,10a-dihydrophenanthrene-3,9-dione) and cDHAs (4′,5-dihydroxy-6′-methoxy-2-methylspiro[cyclohexa[2,5]diene-1,1′-

Novel dihydroquinolizinones for the treatment and prophylaxis of hepatitis B virus infection

The invention provides novel compounds having the general formula: wherein R1, R2, R3, R4, R5 and R6 are as described herein, compositions including the compounds and methods of using the compounds.

NOVEL DIHYDROQUINOLIZINONES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

The invention provides novel compounds having the general formula (I) wherein R1, R2 R3, R4, R5 and R6 are as described herein, compositions including the compounds and methods of using the compounds in the treatment of the hepatitis B virus.

The synthesis and biological activity of two analogs of the anti-HIV alkaloid michellamine B

Two simplified analogs of the dimeric naphthalenyltetrahydroisoquinoline alkaloid michellamine B [4',4''-didesmethoxy-2',2''-didesmethylmichellamine B and 6,8-dihydroxy-5-(1',1''-dihydroxy-2',2''-binaphthalen-4'-yl)-1R,3R-dim ethyl-1,2,3,4-tetrahydroisoqu

Porphyrin synthesis from nitrocompounds

A new porphyrin synthesis starting from nitroalkenes or their equivalents is described. For example, octaethylporphyrin, coproporphyrin, porphyrin-1,2,3,4,5,6,7,8 octapropionic acid, and 2,7,12,17 tetraarylporphyrin are prepared in good yield from readily available materials such as 1-nitropropane, nitroethane, nitromethane, and aldehydes.