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(E)-2-<(4-morpholinylcarbonyl)methyl>-trans-cinnamic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116129-75-0

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116129-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116129-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,2 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116129-75:
(8*1)+(7*1)+(6*6)+(5*1)+(4*2)+(3*9)+(2*7)+(1*5)=110
110 % 10 = 0
So 116129-75-0 is a valid CAS Registry Number.

116129-75-0Relevant academic research and scientific papers

Modular 1,1′-Ferrocenediyl-cored P-Stereogenic Diphosphines: ′′JDayPhos′′ Series and its Use in Rhodium(I)-Catalyzed Hydrogenation

Poklukar, Ga?per,Stephan, Michel,Mohar, Barbara

, p. 2566 - 2570 (2018/05/16)

A novel ferrocene-based P-stereogenic diphospine ligand series dubbed JDayPhos was developed, which rhodium(I) complexes of some of its members exhibited excellent enantioselectivity (up to >99% ee) and high activity in asymmetric hydrogenation of β-unsubstituted or -substituted itaconates and α-methylene-γ-oxo-carboxylates. (Figure presented.).

Renin inhibitors. Dipeptide analogues of angiotensinogen utilizing a structurally modified phenylalanine residue to impart proteolytic stability

Plattner,Marcotte,Kleinert,Stein,Greer,Bolis,Fung,Bopp,Luly,Sham,Kempf,Rosenberg,Dellaria,De,Merits,Perun

, p. 2277 - 2288 (2007/10/02)

A series of renin inhibitors have been prepared and evaluated for their susceptibility to cleavage by the serine protease chymotrypsin. The compounds were designed by consideration of the structural requirements in the active-site region of renin and chymotrypsin. By systematic alteration of the P3 phenylalanine residue, compounds with varying degrees of renin inhibitory potency and chymotrypsin susceptibility were obtained. Selected analogues from this group were examined in vivo for both their hypotensive effects and metabolic patterns.

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