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(1'S,4'R,6'R)-3'-benzyloxycarbonyl-3'-azabicyclo<4.4.0>decan-4'-essigsaeure-methylester is a complex organic compound with a molecular formula of C19H25NO4. It is a derivative of azabicyclo[4.4.0]decane, a bicyclic amine with a nitrogen atom in the ring structure. The compound features a benzyloxycarbonyl group at the 3' position, which is an ester of benzoic acid, and a methyl ester group at the 4' position, derived from acetic acid. The stereochemistry of the compound is defined by the (1'S,4'R,6'R) configuration, indicating the specific arrangement of atoms in the molecule. (1'S,4'R,6'R)-3'-benzyloxycarbonyl-3'-azabicyclo<4.4.0>decan-4'-essigsaeure-methylester is often used in peptide synthesis as a protecting group for the amino group, and it can be found in research and development settings, particularly in the fields of pharmaceuticals and organic chemistry.

76097-51-3

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76097-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76097-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,9 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76097-51:
(7*7)+(6*6)+(5*0)+(4*9)+(3*7)+(2*5)+(1*1)=153
153 % 10 = 3
So 76097-51-3 is a valid CAS Registry Number.

76097-51-3Upstream product

76097-51-3Downstream Products

76097-51-3Relevant academic research and scientific papers

Struktur eines O,N-Ketenacetals: (1RS,8SR,10SR)4(15)Z)-4-Aethyliden-5-oxa-3-azatricyclo3,8>tetradecan)

Kuemin, Albin,Maverick, Emily,Seiler, Paul,Vanier, Noel,Damm, Lorenz,et al.

, p. 1158 - 1175 (1980)

Methods for the preparation of a series of model compounds which were required for stereochemical studies are described: the tricyclic O,N-ketenacetal 1, the two diastereomeric bicyclic amino acids 7 and 10 (see Scheme 2), and the two diastereomeric conformationally fixed tetrahydro-1,3-oxazines (=1,3-oxazines) 9 and 11.An x-ray analysis of racemic 1 reveals a quasi-tetrahedral nitrogen pyramid of the O,N-ketene acetal grouping, and an almost perfect conformational analogy between the N- and C-centered allylic positions at the double bond.

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