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The chemical compound "(1R,2R,6S,7R)-4,4-Dimethyl-8-(toluene-4-sulfonyl)-9-trichloromethyl-3,5-dioxa-8-aza-tricyclo[5.2.1.02,6]decane" is a complex, chiral molecule with a unique structure. It features a tricyclic core with a 3,5-dioxa-8-aza configuration, indicating the presence of two oxygen atoms and a nitrogen atom in the ring. The compound is characterized by its 4,4-dimethyl groups, which are attached to the central carbon atoms of the tricyclic system. A toluene-4-sulfonyl group is attached at the 8-position, providing a sulfonyl functional group that can participate in various chemical reactions. Additionally, a trichloromethyl group is present at the 9-position, which may be involved in electrophilic substitution reactions. The compound's stereochemistry is defined by the (1R,2R,6S,7R) configuration, which specifies the three-dimensional arrangement of the atoms at these positions. This chiral compound has potential applications in the synthesis of pharmaceuticals and other specialty chemicals due to its unique structural features and reactivity.

74202-26-9

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74202-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74202-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,0 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74202-26:
(7*7)+(6*4)+(5*2)+(4*0)+(3*2)+(2*2)+(1*6)=99
99 % 10 = 9
So 74202-26-9 is a valid CAS Registry Number.

74202-26-9Relevant academic research and scientific papers

A CONVENIENT ROUTE TO CARBOCYCLIC ANALOGS OF NUCLEOSIDES: (+/-) ARISTEROMYCIN

Saksena, Anil K.

, p. 133 - 136 (2007/10/02)

Stereocontrolled elaboration of cyclopentadien-azomethine adducts 1 and 2 led to a short total synthesis of (+/-) aristeromycin.In the course of this work a novel zinc reduction was observed.Also, ozonolysis of the gem-dihalo olefin 10 in metha

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