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1H-Isoindole-1-carboxamide, octahydro-(9CI) is a chemical compound with the molecular formula C9H17N2O. It belongs to the class of organic compounds known as isoindole-1-carboxamides, which are derivatives of isoindole, a bicyclic aromatic compound. This specific compound features an octahydro structure, indicating that it contains eight hydrogen atoms in a saturated ring system. The presence of a carboxamide group (-CONH2) in the molecule suggests that it has potential applications in various chemical reactions and may be used as an intermediate in the synthesis of pharmaceuticals or other organic compounds. The compound's unique structure and properties make it an interesting subject for further research and development in the field of organic chemistry.

97039-51-5

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97039-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97039-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,0,3 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97039-51:
(7*9)+(6*7)+(5*0)+(4*3)+(3*9)+(2*5)+(1*1)=155
155 % 10 = 5
So 97039-51-5 is a valid CAS Registry Number.

97039-51-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Octahydro-1H-isoindole-1-carboxamide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:97039-51-5 SDS

97039-51-5Downstream Products

97039-51-5Relevant academic research and scientific papers

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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