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1-Cyclohexene-1-carboxylic acid, 5-amino-3,4-dihydroxy-, (3R,4S,5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

178948-66-8

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178948-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178948-66-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,9,4 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 178948-66:
(8*1)+(7*7)+(6*8)+(5*9)+(4*4)+(3*8)+(2*6)+(1*6)=208
208 % 10 = 8
So 178948-66-8 is a valid CAS Registry Number.

178948-66-8Relevant academic research and scientific papers

Synthesis of aminoshikimic acid

Guo, Jiantao,Frost

, p. 1585 - 1588 (2007/10/03)

5-Amino-5-deoxyshikimic acid (aminoshikimic acid) was synthesized from glucose using recombinant Amycolatopsis mediterranei and also synthesized by a tandem, two-microbe route employing Bacillus pumilus and recombinant Escherichia coli.

Biosynthesis of 3-amino-5-hydroxybenzoic acid, the precursor of mC7N units in ansamycin antibiotics

Kim, Chun-Gyu,Kirschning, Andreas,Bergon, Phillipe,Zhou, Pei,Su, Esther,Sauerbrei, Bernd,Ning, Sandra,Ahn, Yonghyun,Breuer, Michael,Leistner, Eckhard,Floss, Heinz G.

, p. 7486 - 4791 (2007/10/03)

The biosynthetic pathway of 3-amino-5-hydroxybenzoic acid (AHBA) formation was studied with cell-free extracts from the rifamycin B producer, Amycolatopsis mediterranei S699, and the ansatrienin A producer, Streptomyces collinus Tu1892. Phosphoenolpyruvat

Synthesis and evaluation of two new inhibitors of EPSP synthase

Pansegrau, Paul D.,Anderson, Karen S.,Widlanski, Theodore,Ream, Joel E.,Douglas Sammons,Sikorski, James A.,Knowles, Jeremy R.

, p. 2589 - 2592 (2007/10/02)

The enzyme EPSP synthase, EPSPS, (EC 2.5.1.19) catalyzes an unusual transfer reaction of the enolpyruvoyl moiety from phosphoenol pyruvate (2, PEP) regiospecifically to the 5-OH of shikimate 3-phosphate (1, S3P) to form 5-enol-pyruvoylshikimate 3-phosphate (3, EPSP). Two new inhibitors, (4, and 5) were prepared to probe the S3P binding site.

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