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3-(Chloromethyl)-1,4-dimethoxy-2,5-dimethylbenzene is an organic compound with the molecular formula C11H15ClO2. It is a colorless liquid at room temperature and is characterized by its unique chemical structure, which includes a benzene ring with two methyl groups at the 2 and 5 positions, a chloromethyl group at the 3 position, and two methoxy groups at the 1 and 4 positions. 3-(chloromethyl)-1,4-dimethoxy-2,5-dimethylbenzene is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile functional groups, which can be further modified in chemical reactions. It is important to handle 3-(chloromethyl)-1,4-dimethoxy-2,5-dimethylbenzene with care, as it may have potential health and environmental impacts, and appropriate safety measures should be taken during its use and storage.

91244-98-3

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91244-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91244-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,4 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91244-98:
(7*9)+(6*1)+(5*2)+(4*4)+(3*4)+(2*9)+(1*8)=133
133 % 10 = 3
So 91244-98-3 is a valid CAS Registry Number.

91244-98-3Relevant academic research and scientific papers

Photoactivation of amino-substituted 1,4-benzoquinones for release of carboxylate and phenolate leaving groups using visible light

Chen, Yugang,Steinmetz, Mark G.

, p. 6053 - 6060 (2007/10/03)

Upon exposure to visible light, 2-pyrrolidino-substituted 3,6-dimethyl-1,4-benzoquinones photocyclize to give benzoxazolines with quantum yields of 0.07-0.10 in CH2Cl2, 0.02-0.04 in CH 3CN, and 3/su

Photochemical cyclization with release of carboxylic acids and phenol from pyrrolidino-substituted 1,4-benzoquinones using visible light

Chen, Yugang,Steinmetz, Mark G.

, p. 3729 - 3732 (2007/10/03)

(Chemical Equation Presented) Visible light irradiation of 5-acyloxymethyl- and 5-phenoxymethyl-2-pyrrolidino-1,4-benzoquinones effects photoisomerization to labile oxazolidines, which undergo elimination of carboxylate or phenolate leaving groups in high

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