32190-95-7

Usage

Physical Appearance

White or off-white crystalline powder

Solubility

Soluble in water and alcohol

Common Uses

Reagent in organic synthesis
Preparation of pharmaceuticals and dyes
Investigated for potential anti-tumor and anti-inflammatory properties
Production of rubber chemicals
Manufacturing of hair dyes and cosmetics

Safety Considerations

Handle with care
Harmful if ingested or inhaled
May cause irritation to skin and eyes

Upstream product

• 16090-33-8 2-nitrohydroquinone 

Downstream Products

• 54209-92-6 5-hydroxy-2,3-dihydro-1,3-benzoxazol-2-one 
• 1380069-34-0 2-({5-[(2,5-dihydroxyphenyl)carbamoyl]isoxazol-3-yl}oxy)-1-(fluoromethyl)ethyl methanesulfonate 

Relevant academic research and scientific papers

Glucosides from MBOA and BOA detoxification by Zea mays and Portulaca oleracea

Incubation of Zea mays cv. Nicco seedlings with 6-methoxybenzoxazolin-2(3#) -one (MBOA) led to a minor detoxification product hitherto only found in Poaceae. This new compound was identified as 1-(2-hydroxy-4-methoxyphenylamino)- 1-deoxy-β-glucoside 1,2-c

2-[(trifluoroacetyl)amino]benzoquinone and the hydrochloride and perchlorate salts of 2-aminohydroquinone

Hydrogen bonding parameters for the title materials are reported. 2-[(trifluoroacetyl)amino]benzoquinone crystallizes in the monoclinic space group P21/c, with a = 18.195(4), b = 5.110(1), c = 9.635(2), β = 104.22(3)°, V = 868.4(3) A3, and Z = 4. This compound exhibits two weak intramolecular hydrogen bonds. The first is between a hydrogen atom of the quinone ring and the carbonyl oxygen of the trifluoroacetamide group; it has a distance of 2.24 A and a C-H ... O angle of 122°. The second is between the hydrogen atom of the trifluoroacetamide group and a quinone carbonyl group; it has a distance of 2.26 A and a N-H ... O angle of 107°. 2-Aminohydroquinone hydrochloride crystallizes in the orthorhombic space group Pca21, with a = 16.220(3), b = 5.211(1), c = 8.719(2), V = 737.0(2) A3, and Z = 4. 2-Aminohydroquinone perchlorate crystallizes in the orthorhombic space group P212 121, with a = 7.110(1), b = 7.139(1), c= 18.043(4), V = 915.8(3) A3, and Z = 4. All active hydrogens of the two salts exhibit intermolecular hydrogen bonds that serve to organize a three-dimensional framework for each case.

BICYCLIC COMPOUND

The present invention provides to a compound having an ACC inhibitory action, which is useful as an agent for the prophylaxis or treatment of obesity, diabetes, hypertension, hyperlipidemia, cardiac failure, diabetic complications, metabolic syndrome, sarcopenia, cancer and the like, and has superior efficacy. The present invention relates to a compound represented by the formula (I): wherein each symbol is as defined in the specification.