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3,5-diacetyl-1,2,4-trihydroxybenzene is a complex organic compound with the molecular formula C10H10O6. It is a derivative of benzene, featuring three hydroxyl groups (-OH) at the 1, 2, and 4 positions, and two acetyl groups (-COCH3) at the 3 and 5 positions. 3,5-diacetyl-1,2,4-trihydroxybenzene is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates. It is also used in the preparation of certain dyes and pigments due to its ability to form colored compounds. The compound's structure endows it with unique chemical properties, making it a valuable component in advanced chemical research and industrial applications.

2999-24-8

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2999-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2999-24-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,9 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2999-24:
(6*2)+(5*9)+(4*9)+(3*9)+(2*2)+(1*4)=128
128 % 10 = 8
So 2999-24-8 is a valid CAS Registry Number.

2999-24-8Relevant academic research and scientific papers

Synthesis of echinamines A and B, the first aminated hydroxynaphthazarins produced by the sea urchin Scaphechinus mirabilis and its analogues

Pokhilo, Nataly D.,Shuvalova, Maria I.,Lebedko, Maxim V.,Sopelnyak, Galina I.,Yakubovskaya, Alia Ya.,Mischenko, Natalia P.,Fedoreyev, Sergey A.,Anufriev, Victor Ph.

, p. 1125 - 1129 (2006)

The first total synthesis of two marine animated hydroxynaphthazarins, echinamines A (3-amino-7-ethyl-2,5,6,8-tetrahydroxy-1,4-naphthoquinone) and B (2-amino-7-ethyl-3,5,6,8-tetrahydroxy-1,4-naphthoquinone), produced by the sea urchin Scaphechinus mirabil

Pyrans, 84. - Hexahydrobenzotripyrans

Schmiz, Claus,Eiden, Fritz

, p. 2021 - 2030 (2007/10/02)

Catalytic hydrogenation of the benzotripyranone 3 yields the hexahydrobenzotripyrans 5 and 6, while ring closure reactions of the 1,2,4-benzenetriyltris(3-oxypropionic acid) 16c and catalytic hydrogenation lead to the less symmetric isomers 21 and 12.

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