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1,2-cis-2,3-cis-2-acetamidocyclohexane-1,3-diyl diacetate is a complex organic compound with the molecular formula C12H19NO4. It is a derivative of cyclohexane, a cyclic hydrocarbon, with two acetate groups attached to the 1 and 3 positions and an acetamido group at the 2 position. The compound is characterized by its cis configuration, which refers to the spatial arrangement of the acetate and acetamido groups around the cyclohexane ring. This specific geometric isomerism is crucial for its chemical properties and potential applications. The compound is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and the study of stereochemistry. Its unique structure may also have implications in the development of pharmaceuticals or other chemical products that require specific spatial arrangements of functional groups.

3215-07-4

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3215-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3215-07-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,1 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3215-07:
(6*3)+(5*2)+(4*1)+(3*5)+(2*0)+(1*7)=54
54 % 10 = 4
So 3215-07-4 is a valid CAS Registry Number.

3215-07-4Relevant academic research and scientific papers

Stereocontrolled Preparation of Cyclohexane Amino Alcohols Utilising a Modified Mitsunobu Reaction

Sammes, Peter G.,Thetford, Dean

, p. 655 - 661 (2007/10/02)

A method for the introduction of amino groups into aliphatic systems is described.Cyclohex-2-enol reacts with aromatic diacylamines under Mitsunobu reaction conditions to give either N-alkylated or O-alkylated products in a controlled, predictable manner.

NEW ROUTES TO CIS-1,2-HYDROXYAMINES AND RELATED SYSTEMS

Sammes, Peter G.,Thetford, Dean

, p. 2275 - 2278 (2007/10/02)

Use of modified Mitsunobu reactions followed by intramolecular cyclisations have been used to prepare cis-1,2-hydroxyamines, cis-1,3-hydroxyamines, 1,2,3-dihydroxyamines and 1,2,3-diaminoalcohols from allylic alcohols

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