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(S)-ethyl 2-[1-amino-2-(4-benzyloxyphenyl)ethyl]-1,3-oxazole-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

634923-08-3

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634923-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 634923-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,4,9,2 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 634923-08:
(8*6)+(7*3)+(6*4)+(5*9)+(4*2)+(3*3)+(2*0)+(1*8)=163
163 % 10 = 3
So 634923-08-3 is a valid CAS Registry Number.

634923-08-3Downstream Products

634923-08-3Relevant academic research and scientific papers

Solution-phase synthesis of linear and cyclic peptidomimetics based on 2-aminoalkyloxazole-4- Or -5-carboxylates

Cox, Matthew O.,Prager, Rolf H.,Svensson, Carina E.

, p. 747 - 758 (2004)

The solution-phase synthesis of several small linear and cyclic peptidomimetics based on the coupling of BOC-protected 2-aminoalkyloxazole-4- or -5-carboxylic acids is reported. Cyclic amides have been formed both by sequential coupling and cyclization, o

The synthesis of some chiral 2-aminoalkyloxazole-5-carboxylates from isoxazol-5(2H)-ones

Cox, Matthew,Prager, Rolf H.,Svensson, Carina E.,Taylor, Max R.

, p. 897 - 901 (2007/10/03)

Ethyl 5-oxo-2,5-dihydroisoxazole-4-carboxylates have been N-acylated by a number of natural and synthetic phthalimidylamino acids in the presence of carbodiimides. The N-acylated products form the corresponding 2-aminoalkyloxazole-5-carboxylates smoothly when irradiated at 300 nm in acetone.

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