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2-(3,5-bis((2-ethylhexyl)oxy)benzyl)isoindoline-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1147710-40-4

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1147710-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1147710-40-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,7,1 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1147710-40:
(9*1)+(8*1)+(7*4)+(6*7)+(5*7)+(4*1)+(3*0)+(2*4)+(1*0)=134
134 % 10 = 4
So 1147710-40-4 is a valid CAS Registry Number.

1147710-40-4Relevant academic research and scientific papers

One-Component Multifunctional Sequence-Defined Ionizable Amphiphilic Janus Dendrimer Delivery Systems for mRNA

Zhang, Dapeng,Atochina-Vasserman, Elena N.,Maurya, Devendra S.,Huang, Ning,Xiao, Qi,Ona, Nathan,Liu, Matthew,Shahnawaz, Hamna,Ni, Houping,Kim, Kyunghee,Billingsley, Margaret M.,Pochan, Darrin J.,Mitchell, Michael J.,Weissman, Drew,Percec, Virgil

, p. 12315 - 12327 (2021/08/20)

Efficient viral or nonviral delivery of nucleic acids is the key step of genetic nanomedicine. Both viral and synthetic vectors have been successfully employed for genetic delivery with recent examples being DNA, adenoviral, and mRNA-based Covid-19 vaccines. Viral vectors can be target specific and very efficient but can also mediate severe immune response, cell toxicity, and mutations. Four-component lipid nanoparticles (LNPs) containing ionizable lipids, phospholipids, cholesterol for mechanical properties, and PEG-conjugated lipid for stability represent the current leading nonviral vectors for mRNA. However, the segregation of the neutral ionizable lipid as droplets in the core of the LNP, the "PEG dilemma", and the stability at only very low temperatures limit their efficiency. Here, we report the development of a one-component multifunctional ionizable amphiphilic Janus dendrimer (IAJD) delivery system for mRNA that exhibits high activity at a low concentration of ionizable amines organized in a sequence-defined arrangement. Six libraries containing 54 sequence-defined IAJDs were synthesized by an accelerated modular-orthogonal methodology and coassembled with mRNA into dendrimersome nanoparticles (DNPs) by a simple injection method rather than by the complex microfluidic technology often used for LNPs. Forty four (81%) showed activity in vitro and 31 (57%) in vivo. Some, exhibiting organ specificity, are stable at 5 °C and demonstrated higher transfection efficiency than positive control experiments in vitro and in vivo. Aside from practical applications, this proof of concept will help elucidate the mechanisms of packaging and release of mRNA from DNPs as a function of ionizable amine concentration, their sequence, and constitutional isomerism of IAJDs.

A new approach toward light-harvesting reverse micelles from donor-acceptor miscible blends

Takahashi, Masaki,Nishizawa, Natsuko,Ohno, Shuhei,Kakita, Masahiro,Fujita, Norifumi,Yamashita, Mitsuji,Sengoku, Tetsuya,Yoda, Hidemi

experimental part, p. 2669 - 2677 (2009/06/20)

In the present paper, we report a new approach toward light-harvesting reverse micellar systems from molecular blends of anthracene and perylene building blocks. The self-assembly initiated by protonation of the molecular blends gave rise to the mixed rev

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