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1H-Isoindole-1-carbonitrile, octahydro-, (1α,3aα,7aα)-(9CI) is a chemical compound with the molecular formula C10H15N. It is a derivative of isoindole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to a pyrrolidine ring. The octahydro prefix indicates that the compound has undergone hydrogenation, resulting in the saturation of its double bonds. The (1α,3aα,7aα)-(9CI) notation specifies the stereochemistry of the compound, with the α-configuration at the 1st, 3a, and 7a positions. This particular chemical is used as an intermediate in the synthesis of various pharmaceuticals and other organic compounds, due to its unique structure and reactivity.

96798-41-3

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96798-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96798-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,9 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 96798-41:
(7*9)+(6*6)+(5*7)+(4*9)+(3*8)+(2*4)+(1*1)=203
203 % 10 = 3
So 96798-41-3 is a valid CAS Registry Number.

96798-41-3Downstream Products

96798-41-3Relevant academic research and scientific papers

ANTIVIRAL COMPOUNDS FOR THE TREATMENT OF CORONAVIRUS, PICORNAVIRUS AND NOROVIRUS INFECTIONS

-

, (2021/12/31)

Provided herein are compounds of Formula (I), or pharmaceutically acceptable salts thereof, pharmaceutical compositions that include a compound described herein (including pharmaceutically acceptable salts of a compound described herein) and methods of synthesizing the same. Also provided herein are methods of treating coronavirus, Picomavirus and Norovims infections with a compound of Formula (I), or a pharmaceutically acceptable salt thereof.

Enantioselective biocatalytic oxidative desymmetrization of substituted pyrrolidines

Koehler, Valentin,Bailey, Kevin R.,Znabet, Anass,Raftery, James,Helliwell, Madeleine,Turner, Nicholas J.

supporting information; experimental part, p. 2182 - 2184 (2010/06/18)

"Chemical Equation Presented" Center stage: Additions of nitrogen-centered radicals to cyanamide compounds provided the first radical synthesis of aromatic polycyclic guanidine derivatives (see scheme). Modular assembly of the substrates allows for a rapid increase of the molecular complexity of scaffolds, which have potential applications for medicinal chemistry.

OXYDATION OF SECONDARY AMINES TO α-CYANOAMINES

Barton, Derek H. R.,Billion, Annick,Boivin, Jean

, p. 1229 - 1232 (2007/10/02)

The dehydrogenation of secondary amines with phenylseleninic anhydride or acid under mild conditions in the presence of either sodium cyanide or trimethylsilylcyanide gives good yields of α-cyanoamines.These compounds can be regarded as protected imines, or as a source of α-amino-acids.

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