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N-Benzoyl-N-(S)-α-phenaethyl-(S)-valin-tert-butylamid is a complex organic compound with the molecular formula C22H28N2O3. It is a derivative of valine, an essential amino acid, and is characterized by the presence of a benzoyl group, a phenethyl group, and a tert-butylamide group. N-Benzoyl-N-(S)-α-phenaethyl-(S)-valin-tert-butylamid is often used in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is typically used in its (S)-enantiomeric form, which is the naturally occurring form of the compound. The compound's specific structure and properties make it a valuable building block in the development of new drugs and other chemical products.

6397-99-5

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6397-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6397-99-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,9 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6397-99:
(6*6)+(5*3)+(4*9)+(3*7)+(2*9)+(1*9)=135
135 % 10 = 5
So 6397-99-5 is a valid CAS Registry Number.

6397-99-5Downstream Products

6397-99-5Relevant academic research and scientific papers

Ugi four component condensations using aldehydes with an asymmetric centre at C-2

Kelly,Lawrie,Morgan,Willis

, p. 8001 - 8005 (2007/10/03)

Epimerisation of an aldehyde possessing a hydrocarbon substituent α to the carbonyl occurs in the Ugi four component condensation whereas, with either a benzyl or TBDMS ether at C-2 the stereochemical integrity is maintained. A deuterium isotope effect is observed and by carrying out the reaction in methanol-OD, deuterium can be introduced efficiently into C-3 of the condensation products. (C) 2000 Elsevier Science Ltd.

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