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78793-09-6

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78793-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78793-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,9 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78793-09:
(7*7)+(6*8)+(5*7)+(4*9)+(3*3)+(2*0)+(1*9)=186
186 % 10 = 6
So 78793-09-6 is a valid CAS Registry Number.
InChI:InChI=1/C26H46N2O4/c1-15(4-7-23(32)28-11-10-27)18-5-6-19-24-20(14-22(31)26(18,19)3)25(2)9-8-17(29)12-16(25)13-21(24)30/h15-22,24,29-31H,4-14,27H2,1-3H3,(H,28,32)/t15-,16+,17-,18+,19+,20+,21-,22+,24+,25+,26-/m1/s1

78793-09-6Downstream Products

78793-09-6Relevant articles and documents

THE PREPARATION OF AMINO BILE ACID DERIVATIVES

Hill, A.,Ross, P. E.,Bouchier, I. A. D.

, p. 393 - 398 (1981)

Bile acid derivatives have been prepared by reaction of their mixed anhydrides with diaminoethane.The new compounds have side chains modified by amide bond formation which extends the side chain by two carbon atoms and terminates in a primary amino group.

Synthesis of a head to head cholaphane

Pandey, Pramod S.,Singh, Rhiddi Bir

, p. 5045 - 5046 (1997)

A general synthetic route for the construction of head to head cholaphanes, a new type of steroidal macrocycles, has been described.

Synthesis of new cisplatin derivatives from bile acids

?otowski, Zenon,Hryniewicka, Agnieszka,Morzycki, Jacek W.,Rárová, Lucie,Seroka, Barbara,Sicinski, Rafal R.,Tomkiel, Aneta M.

, (2020/02/18)

A series of bile acid derived 1,2- and 1,3-diamines as well as their platinum(II) complexes were designed and synthesized in hope to get a highly cytotoxic compound by the combination of two bioactive moieties. All complexes obtained were subjected to cytotoxicity assays in vitro and some hybrid molecules showed an expected activity.

Glycogen phosphorylase inhibitor and preparation method and application thereof

-

Paragraph 0056; 0057; 0058; 0059, (2017/01/02)

The invention belongs to the technical field of drug synthesis and discloses a glycogen phosphorylase inhibitor and a preparation method and application thereof. The gGlycogen phosphorylase inhibitor has a structural general formula shown as a formula (1)

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