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1,2-trans-2,3-cis-3-acetamidocyclohexane-1,2-diyl diacetate is a complex organic compound with the molecular formula C12H19NO4. It is a derivative of cyclohexane, a cyclic hydrocarbon, with acetamide and acetate functional groups. The compound features a trans configuration between the first and second carbon atoms and a cis configuration between the second and third carbon atoms. The 3-acetamido group is attached to the cyclohexane ring, and two acetate groups are connected to the first and second carbon atoms, respectively. This chemical is primarily used in the synthesis of various pharmaceuticals and biologically active compounds due to its unique structure and reactivity. Its properties, such as solubility and stability, can be influenced by the specific arrangement of functional groups and the overall molecular geometry.

2630-68-4

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2630-68-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2630-68-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,3 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2630-68:
(6*2)+(5*6)+(4*3)+(3*0)+(2*6)+(1*8)=74
74 % 10 = 4
So 2630-68-4 is a valid CAS Registry Number.

2630-68-4Downstream Products

2630-68-4Relevant academic research and scientific papers

Desymmetrization of hydrazinocyclohexadienes: A new approach for the synthesis of polyhydroxylated aminocyclohexanes

Errastl, Gauthier,Kounde, Cyrille,Mlrguet, Olivier,Lecourt, Thomas,Micouln, Laurent

supporting information; experimental part, p. 2912 - 2915 (2009/12/06)

Hydrazlnocyclohexadlenes, easily prepared by an ene-reactlon between commercially available azodlcarboxylate reagents and cyclohexadlene, are Interesting substrates for desymmetrlzatlon reactions. Under Sharpless asymmetric dihydroxylation conditions, the

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

Synthetic Study and Conformational Analysis of O-Benzylated Aminocyclitols

Kiso, Makoto,Kobayashi, Toshiyuki,Hasegawa, Akira

, p. 419 - 426 (2007/10/02)

DL-(1,3/2)-3-Acetamido-1,2-di-O-benzylcyclohex-4-enediol (IIIa) and DL-(1,3/4)-1-acetamido-3,4-di-O-benzylcyclohex-5-enediol (IIIb) were synthesized from DL-trans-1,2-di-O-benzylcyclohex-3-enediol (I) via the corresponding azide derivatives (IIa-b) prepar

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