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Allyloxypropanol, also known as 3-allyloxy-1-propanol or allyl glycidyl ether, is a colorless liquid with a molecular formula of C6H12O2. It is an organic compound that is primarily used as a chemical intermediate in the synthesis of various products, such as pharmaceuticals, agrochemicals, and specialty chemicals. Allyloxypropanol is characterized by its reactive epoxy group and allyl group, which allows it to participate in various chemical reactions, including ring-opening polymerization and addition reactions. Due to its reactivity, it is essential to handle allyloxypropanol with caution, as it can be harmful if inhaled, ingested, or absorbed through the skin.

6180-67-2

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6180-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6180-67-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,8 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6180-67:
(6*6)+(5*1)+(4*8)+(3*0)+(2*6)+(1*7)=92
92 % 10 = 2
So 6180-67-2 is a valid CAS Registry Number.

6180-67-2Relevant academic research and scientific papers

PRODUCTION PROCESS OF 3-ALKOXY-1-PROPANOLS, AND 3-ALKOXY-1-PROPANOLS OBTAINED BY THE PRODUCTION PROCESS

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Page/Page column 35-36; 54, (2008/06/13)

In the presence of a catalyst containing at least one element selected from the group consisting of elements of the group III, lanthanoid elements and actinoid elements of the Periodic Table, an allyl alcohol is reacted with an alcohol compound. A method for efficiently producing 3-alkoxy-1-propanol in a single step using an alcohol as a starting material is provided.

Selective cleavage of allyl ethers

Lee, Jinhwa,Cha, Jin Kun

, p. 3663 - 3666 (2007/10/03)

A simple, one-step method for the selective cleavage of allyl ethers to alcohols has been developed by use of Ti(O-i-Pr)4 and a commercially available Grignard reagent.

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