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1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)ethan-1-ol is a complex organic compound with the molecular formula C10H12O3. It is a derivative of benzo[b][1,4]dioxin, which is a type of dibenzo-p-dioxin. 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)ethan-1-ol features a benzene ring with two oxygen atoms forming a dioxin ring, and a 2,3-dihydro structure, which means that one of the double bonds in the benzene ring has been reduced to a single bond. The molecule also contains an ethanol group attached to the 1-position of the benzene ring. This chemical is primarily of interest in the field of organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and other chemical compounds. However, due to its complex structure and potential toxicity, it is important to handle 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)ethan-1-ol with caution and in accordance with proper safety protocols.

7338-03-6

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7338-03-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7338-03-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7338-03:
(6*7)+(5*3)+(4*3)+(3*8)+(2*0)+(1*3)=96
96 % 10 = 6
So 7338-03-6 is a valid CAS Registry Number.

7338-03-6Relevant academic research and scientific papers

Direct synthesis of ethers from aldehydes and ketones. One-pot reductive etherification of benzaldehydes, alkyl aryl ketones, and benzophenones

Mochalov,Fedotov,Trofimova,Zefirov

, p. 503 - 512 (2016)

Benzyl alcohols formed by the reduction of benzaldehydes, alkyl aryl ketones, and benzophenones with sodium tetrahydridoborate in alcohols undergo in situ etherification with the solvent in the presence of a catalytic amount of HCl. Thus the process may be regarded as one-pot transformation of carbonyl compounds into the corresponding benzyl ethers. The yields of ethers depend on the substituent nature in the aromatic fragment of the initial carbonyl compound and on the alcohol used as reduction medium.

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