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(-)-(3R,4R)-5-benzyloxycarbonyl-2-(4-methoxyphenyl)-3-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,5-diazaspiro[3.4]octan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

729599-78-4

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729599-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 729599-78-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,9,5,9 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 729599-78:
(8*7)+(7*2)+(6*9)+(5*5)+(4*9)+(3*9)+(2*7)+(1*8)=234
234 % 10 = 4
So 729599-78-4 is a valid CAS Registry Number.

729599-78-4Relevant academic research and scientific papers

N-heterocyclic carbene catalyzed ring expansion of 4-formyl-β-lactams: Synthesis of succinimide derivatives

Li, Gong-Qiang,Li, Yi,Dai, Li-Xin,You, Shu-Li

, p. 3519 - 3521 (2008/02/11)

N-Heterocyclic carbene (NHC) has been employed as an efficient catalyst for ring expansion of 4-formyl-β-lactams, allowing the facile synthesis of succinimide derivatives. This organocatalytic process features readily availability of the catalyst, low cat

Unusual rearrangement of spiro β-lactams to 1,4-diazabicyclo[4,4,0] decanes and 1,4-diazabicyclo[4,3,0]nonanes. Synthesis of conformationally restricted σ-receptor ligands

Macías, Alberto,Alonso, Eduardo,Del Pozo, Carlos,González, Javier

, p. 4657 - 4660 (2007/10/03)

Synthesis of 1,4-diazabicyclo[4,4,0]decanes and 1,4-diazabicyclo[4,3,0] nonanes was achieved by using 4-formyl spiro β-lactams as easily available starting materials. Furthermore, the application of this protocol to the preparation of conformationally res

Diastereoselective [2+2]-cycloaddition reactions of unsymmetrical cyclic ketenes with imines: Synthesis of modified prolines and theoretical study of the reaction mechanism

Macias, Alberto,Alonso, Eduardo,Del Pozo, Carlos,Venturini, Alessandro,Gonzalez, Javier

, p. 7004 - 7012 (2007/10/03)

The synthesis of enantiomerically pure modified proline derivatives was achieved by using spiro β-lactams as starting material that were prepared in turn by the [2+2]-cycloaddition of unsymmetrical cyclic ketenes with optically active imines. A theoretica

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