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3,12-dihydroxy-9(10)-secoandrosta-1,3,5(10)-triene-9,17-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79683-94-6

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79683-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79683-94-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,8 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79683-94:
(7*7)+(6*9)+(5*6)+(4*8)+(3*3)+(2*9)+(1*4)=196
196 % 10 = 6
So 79683-94-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H24O4/c1-11-3-5-13(20)9-12(11)4-6-14-15-7-8-17(22)19(15,2)18(23)10-16(14)21/h3,5,9,14-15,18,20,23H,4,6-8,10H2,1-2H3/t14-,15-,18+,19-/m0/s1

79683-94-6Downstream Products

79683-94-6Relevant academic research and scientific papers

Phenolic 9,10-secosteroids as products of the catabolism of bile acids by a Pseudomonas sp.

Park, R. J.

, p. 175 - 194 (2007/10/02)

The obligate aerobe, Pseudomonas putida ATCC 31752, efficiently utilises bile acids as a source of carbon and energy for growth and maintenance.When aeration is considerably restricted, a consequence to the catabolism of the bile acids in a fermentor is an accumulation of certain steroidal catabolites.Evidence is presented to show that among these are hydroxy-9,10-seco-1,3,5(10)-androstatriene-9,17-diones and those from four of the common bile acids, cholic, chenodeoxycholic, hyodeoxycholic and deoxycholic acids have been isolated and their structures determined.The product of catabolism of hyodeoxycholic acid appears to exist in a hemi-acetal form which readily forms an acetal during isolation procedures.All but one of these are described for the first time.

DEOXYCHOLIC ACID DEGRADATION BY A PSEUDOMONAS SP: PHENOLIC AND NEUTRAL PRODUCTS

Leppik, R. A.

, p. 1747 - 1751 (2007/10/02)

The microbial degradation of deoxycholic acid by Pseudomonas sp.MR108 was studied, and four products were isolated.Evidence is presented that one is the phenol 3,12β-dihydroxy-9,10-secoandrosta-1,3,5(10)-trien-9,17-dione (11) and that the other three are the neutral compounds 3aαH-4α--5α-hydroxy-7aβ-methyl-hexahydro-1-indanone-δ-lactone (12), 12β-hydroxyandrosta-1,4-dien-3,17-dione (10), and 12α-hydroxyandrosta-1,4-dien-3,17-dione (7).

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