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3-(4-azidophenoxy) propyl methanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

943726-04-3

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943726-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943726-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,7,2 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 943726-04:
(8*9)+(7*4)+(6*3)+(5*7)+(4*2)+(3*6)+(2*0)+(1*4)=183
183 % 10 = 3
So 943726-04-3 is a valid CAS Registry Number.

943726-04-3Downstream Products

943726-04-3Relevant articles and documents

A benzenesulfonamide derivative as a novel PET radioligand for CXCR4

Goodman, Mark M.,Liang, Zhongxing,Oum, Yoon Hyeun,Shetty, Dinesh,Shim, Hyunsuk,Voll, Ronald J.,Yoon, Younghyoun

, (2020)

CXCR4 is involved in various diseases such as inflammation, tumor growth, and cancer metastasis through the interaction with its natural endogenous ligand, chemokine CXCL12. In an effort to develop imaging probes for CXCR4, we developed a novel small mole

METHYLSULFONAMIDE DERIVATIVES AND USES RELATED THERETO

-

Page/Page column 73-74, (2017/02/28)

This disclosure relates to methylsulfonamide derivatives and uses as imaging agents and other uses related to CXCR4 inhibition. In certain embodiments, the disclosure relates to pharmaceutical compositions comprising compounds disclosed herein, derivative

An efficient F-18 labeling method for PET study: Huisgen 1,3-dipolar cycloaddition of bioactive substances and F-18-labeled compounds

Sirion, Uthaiwan,Kim, Hee Jun,Lee, Jae Hak,Seo, Jai Woong,Lee, Byoung Se,Lee, Sang Ju,Oh, Seung Jun,Chi, Dae Yoon

, p. 3953 - 3957 (2008/02/04)

The Cu(I)-catalyzed, 1,3-dipolar cycloaddition reaction was applied successfully to the synthesis of small, F-18-labeled biomolecules, and an optimal condition was developed for one-pot, two-step reaction without any interim purifications. This technique was employed in various F-18-labeled, 1,2,3-triazole syntheses with high radiochemical yield.

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