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1529807-51-9

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1529807-51-9 Usage

General Description

[14C]-methyl-[(2,5-dichlorobenzoyl)amino]acetate is a radio-labeled compound used in biochemical and pharmacological research. It is a derivative of the amino acid glycine, with a methyl group and a dichlorobenzoyl group attached to the amino group of glycine. The presence of the radio-labeled carbon-14 allows for tracking and tracing the compound in biological systems. This chemical is commonly used in experiments to study the metabolism, absorption, distribution, and excretion of drugs and other compounds in living organisms. Additionally, it can be utilized in the synthesis of pharmaceuticals and in the investigation of enzyme activity and kinetics.

Check Digit Verification of cas no

The CAS Registry Mumber 1529807-51-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,9,8,0 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1529807-51:
(9*1)+(8*5)+(7*2)+(6*9)+(5*8)+(4*0)+(3*7)+(2*5)+(1*1)=189
189 % 10 = 9
So 1529807-51-9 is a valid CAS Registry Number.

1529807-51-9Relevant articles and documents

Syntheses of C-13 and C-14-labeled versions of the investigational proteasome inhibitor MLN9708

Plesescu, Mihaela,Elliott, Eric L.,Li, Yuexian,Prakash, Shimoga R.

, p. 464 - 470 (2014/03/21)

MLN9708 (ixazomib citrate) is an investigational, orally bioavailable proteasome inhibitor that is under development by Millennium in clinical studies in both hematologic and nonhematologic malignancies. The stable isotope-labeled MLN9708 was required for bio-analytical studies. [13C 9]-MLN9708 (11) was synthesized in seven steps from the uniformly labeled [13C6]-1,4-dichlorobenzene (3) and [1- 13C]-acetyl chloride. Because of the presence of two chlorine atoms and a boron atom, compound 6 was further reacted with [13C 2]-glycine to provide an internal standard that is well separated from the parent compound during mass spectrometric analysis. The radiolabeled version was prepared to support metabolite profiling and whole body autoradiography studies in experimental animals. [14C]-MLN9708 (19) was synthesized in six steps from commercially available [14C]-barium carbonate. The key intermediate, [carboxyl-14C]-2,5-dichlorobenzoic acid (14), was prepared by selective lithiation of 1-bromo-2,5-dichlorobenzene (12) followed by carbonation with [14C]-barium carbonate. In preparation for a one-time human absorption, distribution, metabolism and excretion (ADME) study, the stability of [14C]-MLN9708 and its precursors were also evaluated. Copyright

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