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DL-(1,3,5/2,4)-1-Acetamido-2,3,4,5-tetra-O-acetylcyclohexanetetrol is a complex organic compound with the molecular formula C16H23NO8. It is a derivative of cyclohexane, a six-carbon ring structure, with four hydroxyl groups (-OH) at positions 2, 3, 4, and 5, and an acetamido group (-NHCOCH3) at position 1. The compound is characterized by the presence of four acetyl groups (-COCH3), which are attached to the hydroxyl groups, making it a tetra-O-acetyl derivative. This chemical is synthesized for various applications in organic chemistry, such as a building block for more complex molecules or as an intermediate in the synthesis of pharmaceuticals. Its structure and properties make it a versatile compound in the field of chemical research and development.

6216-28-0

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6216-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6216-28-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6216-28:
(6*6)+(5*2)+(4*1)+(3*6)+(2*2)+(1*8)=80
80 % 10 = 0
So 6216-28-0 is a valid CAS Registry Number.

6216-28-0Relevant academic research and scientific papers

6-Exo Free Radical Cyclization of Acyclic Carbohydrate Intermediates: A New Synthetic Route to Enantiomerically Pure Polyhydroxylated Cyclohexane Derivatives

Marco-Contelles, Jose,Pozuelo, Carmen,Jimeno, M. L.,Martinez, Luis,Martinez-Grau, Angeles

, p. 2625 - 2631 (2007/10/02)

The 6-exo free radical cyclization of conveniently functionalized acyclic carbohydrate derivatives is a new and efficient method for the asymmetric synthesis of polyhydroxylated cyclohexane compounds (aminocyclitols, pseudosugars).The scope and versatilit

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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