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(1S,2S,4R,5R,6S,7S)-3-Oxa-tricyclo[3.2.1.02,4]octane-6,7-dicarboxylic acid is a complex organic compound with a unique cyclic structure. It consists of a tricyclic ring system with a three-carbon ring fused to a two-carbon ring, which is further fused to another three-carbon ring. The molecule contains an oxygen atom (oxa) in the middle of the structure, and two carboxylic acid groups attached to the 6th and 7th carbon atoms. The stereochemistry of the compound is defined by the R and S configurations at each chiral center, indicating the specific three-dimensional arrangement of the atoms. (1S,2S,4R,5R,6S,7S)-3-Oxa-tricyclo[3.2.1.02,4]octane-6,7-dicarboxylic acid is known for its potential applications in pharmaceuticals and as a building block in the synthesis of various biologically active molecules.

6004-78-0

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6004-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6004-78-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6004-78:
(6*6)+(5*0)+(4*0)+(3*4)+(2*7)+(1*8)=70
70 % 10 = 0
So 6004-78-0 is a valid CAS Registry Number.

6004-78-0Relevant academic research and scientific papers

Enzymatic optical resolution of norbornanecarboxylic esters using Pig Liver Esterase

Gastel, F. J. C. van,Klunder, A. J. H.,Zwanenburg, B.

, p. 175 - 184 (2007/10/02)

The hydrolysis of a series of norbornane-type carboxylic esters catalyzed by pig liver esterase (PLE) has been investigated.It was found that an exo-ester function (syn to the C7 methylene group) is hydrolyzed with high preference.Enantioselective hydrolysis can be accomplished when a vicinal carbonyl-containing function (ester, formyl, acetyl) is present in a trans position with respect to the exo ester.The regiospecifity of the enzymatic hydrolysis has been used for the separation of exo/endo mixtures of the cycloadducts derived from cyclopentadiene and alkene esters.The regiospecifity and enantioselectivity of the enzymatic hydrolysis of norbornane-type esters were analyzed in terms of Tamm's substrate model and also by Griengl's method.

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