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Tetrahydrofuran-2-propanol acetic acid ester, also known as 2-(2-tetrahydrofuryl)-1-ethanol acetate, is a chemical compound derived from the esterification of 2-(2-tetrahydrofuryl)-1-ethanol and acetic acid. This organic ester is characterized by a tetrahydrofuran ring and a propanol group, which contribute to its unique chemical properties. It is a colorless liquid with a specific boiling point and is soluble in various organic solvents. tetrahydrofuran-2-propanol acetic acid ester is primarily used as a solvent in the chemical industry, particularly in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Its ability to dissolve a wide range of substances makes it a versatile component in many industrial processes.

772-77-0

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772-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 772-77-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 772-77:
(5*7)+(4*7)+(3*2)+(2*7)+(1*7)=90
90 % 10 = 0
So 772-77-0 is a valid CAS Registry Number.

772-77-0Downstream Products

772-77-0Relevant academic research and scientific papers

Stereoselective ring expansion via bicyclooxonium ion. A novel approach to oxocanes

Sakamoto, Yasuharu,Tamegai, Kyoko,Nakata, Tadashi

, p. 675 - 678 (2002)

(equation presented) The stereoselective 1,4-rearrangement-ring expansion of tetrahydrofurans via bicyclo[3.3.0]oxonium ions was developed to synthesize oxocanes. On the basis of this rearrangement, the stereoselective synthesis of 2,8-syn-2,8-dimethyloxo

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