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1(3H)-Isobenzofuranone, 3-(3,5-dimethoxyphenyl)-4,5-dimethoxy-7-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90359-82-3

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90359-82-3 Usage

Type

Chemical compound

Occurrence

Naturally occurring in certain plants, including nutmeg and mace

Pharmacological Properties

a. Anti-inflammatory effects
b. Antimicrobial effects

Psychoactive Properties

Known for its hallucinogenic effects

Traditional Use

Used in some cultures for its psychoactive properties

Toxicity

Considered toxic and potentially harmful

Precaution

Caution should be exercised when handling or using 1(3H)-Isobenzofuranone, 3-(3,5-dimethoxyphenyl)-4,5-dimethoxy-7-methyl-

Check Digit Verification of cas no

The CAS Registry Mumber 90359-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,5 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90359-82:
(7*9)+(6*0)+(5*3)+(4*5)+(3*9)+(2*8)+(1*2)=143
143 % 10 = 3
So 90359-82-3 is a valid CAS Registry Number.

90359-82-3Relevant academic research and scientific papers

Directed Metalation of N,N-Diethylbenzamides. Silylated Benzamides for the Synthesis of Naturally Occurring pero-Methylanthraquinones and peri-Methyl Polycyclic Aromatic Hydrocarbons

Mills, Robert J.,Snieckus, Victor

, p. 4386 - 4390 (2007/10/02)

Efficient methodologies based on directed ortho metalation, fluoride-induced carbodesilylation, and metal-halogen exchange processes (Scheme I) are reported for the synthesis of peri-methyl-substituted anthraquinone natural products 5 and polycyclic aroma

SILICON IN BENZAMIDE DIRECTED ORTHO METALATION REACTIONS. CARBO- AND BROMO-DESILYLATIONS AND SYNTHESIS OF NATURALLY-OCCURING ANTHRAQUINONES

Mills, R.J.,Snieckus, V.

, p. 483 - 486 (2007/10/02)

Silylated benzamides 2, avaible by directed ortho metalation, undergo fluorideinduced carbodesilylation and ipso bromodesilylation to give usefully-substituted aromatics 3 and 4; these reactions are utilized in a short and efficient synthesis of erythrola

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