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tert-butyl 4-hydroxy-3,5-diiodobenzylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1404213-19-9

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1404213-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1404213-19-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,4,2,1 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1404213-19:
(9*1)+(8*4)+(7*0)+(6*4)+(5*2)+(4*1)+(3*3)+(2*1)+(1*9)=99
99 % 10 = 9
So 1404213-19-9 is a valid CAS Registry Number.

1404213-19-9Relevant articles and documents

Design, synthesis, and biological evaluation of novel bifunctional thyrointegrin antagonists for neuroblastoma

Karakus, Ozlem Ozen,Godugu, Kavitha,Fujioka, Kazutoshi,Mousa, Shaker A.

, (2021)

Receptor-mediated cancer therapy has received much attention in the last few decades. Neuroblastoma and other cancers of the sympathetic nervous system highly express norepinephrine transporter (NET) and cell plasma membrane integrin αvβ3. Dual targeting

SUBSTITUTED 4-PHENOXYPHENOL ANALOGS AS MODULATORS OF PROLIFERATING CELL NUCLEAR ANTIGEN ACTIVITY

-

, (2013/03/26)

In one aspect, the invention relates to substituted 4-phenoxyphenol analogs, derivatives thereof, and related compounds,which are useful as inhibitors of proliferating cell nuclear antigen (PCNA); synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating hyperproliferative disorders associated with PCNA using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention

Studies toward the synthesis of phenylacetylene macrocycle based rotaxane precursors as building blocks for organic nanotubes

Cantin, Katy,Lafleur-Lambert, Antoine,Dufour, Philippe,Morin, Jean-Francois

, p. 5335 - 5349 (2012/10/30)

Synthetic efforts toward the preparation of rotaxane precursors based on phenylacetylene macrocycles (PAM) are described. The aim of this study was to determine the optimal structural parameters to prepare high-molecular-weight rotaxane precursors through a strategy involving two Sonogashira couplings to attach bulky blockers on the PAM core. PAMs with different sizes and functions were prepared and coupled to different blockers to assess whether or not the resulting structure adopts a rotaxane-like conformation in which the rigid rod forms after the Sonogashira coupling threads through the PAM. Copyright

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