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1,3,5-trichloro-2,4,6-trimethoxybenzene is an organic compound with the chemical formula C9H9Cl3O3. It is a derivative of benzene, featuring three chlorine atoms at the 1, 3, and 5 positions, and three methoxy groups at the 2, 4, and 6 positions. 1,3,5-trichloro-2,4,6-trimethoxybenzene is characterized by its symmetrical structure and halogenated aromatic properties. It is typically synthesized through the reaction of benzene with chlorinating agents and methanol under specific conditions. Due to its unique structure, 1,3,5-trichloro-2,4,6-trimethoxybenzene has potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, where its chemical properties can be exploited for specific purposes.

1015-96-9

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1015-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1015-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1015-96:
(6*1)+(5*0)+(4*1)+(3*5)+(2*9)+(1*6)=49
49 % 10 = 9
So 1015-96-9 is a valid CAS Registry Number.

1015-96-9Downstream Products

1015-96-9Relevant academic research and scientific papers

Lanosta-8,17,25-trien-3β-ol and isomeric trichlorotrimethoxybenzenes from Fomes fastuosus

Jain, Subhash C.,Kumar, Ravindra,Gupta, Bhavna,Olsen, Carl E.

, p. 2200 - 2202 (2007/10/03)

Phytochemical investigation of the fungus, F. fastuosus has led to the isolation of a new triterpene, lanosta-8,17,25-trien-3β-ol 1 and two isomeric trichlorotrimethoxybenzenes, viz., 1,2,3-trichloro-4,5,6-trimethoxybenzene 2 and 1,2,4-trichloro-3,5,6-tri

Facile Synthesis of Chloro-substituted Aromatic Ethers by Use of Benzyltrimethylammonium Tetrachloroiodate

Kajigaeshi, Shoji,Shinmasu, Youichi,Fujisaki, Shizuo,Kakinami, Takaaki

, p. 415 - 418 (2007/10/02)

The reaction of aromatic ethers with a calculated amount of benzyltrimethylammonium tetrachloroiodate in acetic acid (or dichloromethane) under mild conditions gave, selectively, the objective chloro-substituted aromatic ethers in good yields.

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