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5-(prop-2-ynyloxy)isophthaloyl dichloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1114540-72-5

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1114540-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1114540-72-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,4,5,4 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1114540-72:
(9*1)+(8*1)+(7*1)+(6*4)+(5*5)+(4*4)+(3*0)+(2*7)+(1*2)=105
105 % 10 = 5
So 1114540-72-5 is a valid CAS Registry Number.

1114540-72-5Relevant academic research and scientific papers

Ion-pair recognition of amidinium salts by partially hydrogen-bonded heteroditopic cyclo[6]aramide

Shi, Shanshan,Zhu, Yumin,Li, Xiaowei,Yuan, Xiangyang,Ma, Teng,Yuan, Wen-Li,Tao, Guo-Hong,Feng, Wen,Yuan, Lihua

, p. 39839 - 39845 (2016)

Convergent heteroditopic cyclo[6]aramide demonstrates efficient ion-pair recognition of amidinium salts in 10% methanolic chloroform (>104 M-1) as confirmed by NMR and conductivity experiments. As predicted by density functional theo

Non-Covalently Pre-Assembled High-Performance Near-Infrared Fluorescent Molecular Probes for Cancer Imaging

Shaw, Scott K.,Liu, Wenqi,Gómez Durán, César Fernando Azael,Schreiber, Cynthia L.,Betancourt Mendiola, María de Lourdes,Zhai, Canjia,Roland, Felicia M.,Padanilam, Simon J.,Smith, Bradley D.

supporting information, p. 13821 - 13829 (2018/09/14)

New fluorescent molecular probes, which can selectively target specific cell surface receptors, are needed for microscopy, in vivo imaging, and image guided surgery. The preparation of multivalent probes using standard synthetic chemistry can be a laborious process due to low reaction yields caused by steric effects. In this study, fluorescent molecular probes were prepared by a programmed non-covalent pre-assembly process that used a near-infrared fluorescent squaraine dye to thread a macrocycle bearing a cyclic arginine-glycine-aspartate peptide antagonist (cRGDfK) as a cancer targeting unit. Cell microscopy studies using OVCAR-4 (ovarian cancer) and A549 (lung cancer) cells that express high levels of the integrin αvβ3 or αvβ5 receptors, respectively, revealed a multivalent cell targeting effect. That is, there was comparatively more cell uptake of a pre-assembled probe equipped with two copies of the cRGDfK antagonist than a pre-assembled probe with only one appended cRGDfK antagonist. The remarkably high photostability and low phototoxicity of these near-infrared probes allowed for acquisition of long-term fluorescence movies showing endosome trafficking in living cells. In vivo near-infrared fluorescence imaging experiments compared the biodistribution of a targeted and untargeted probe in a xenograft mouse tumor model. The average tumor-to-muscle ratio for the pre-assembled targeted probe was 3.6 which matches the tumor targeting performance reported for analogous cRGDfK-based probes that were prepared entirely by covalent synthesis. The capability to excite these pre-assembled near-infrared fluorescent probes with blue or deep-red excitation light makes it possible to determine if a target site is located superficially or buried in tissue, a probe performance feature that is likely to be very helpful for eventual applications such as fluorescence guided surgery.

A new thermo- and photo-driven [2]rotaxane

Ji, Feng-Yuan,Zhu, Liang-Liang,Ma, Xiang,Wang, Qiao-Chun,Tian, He

supporting information; experimental part, p. 597 - 600 (2009/05/27)

A new rotaxane with functional chromophores porphyrin and fluorene as stoppers has been synthesized. It displays dual fluorescent character. The macrocycle ring can shuttle between the fumaramide part and the succinimide part on the dumbbell. Heating and UV light irradiating on the rotaxane lead to the reversible E/Z conversion, driving the ring to shuttle between the two stations. The optical properties of porphyrin and fluorene stoppers of the thread do not change so much while the ring shuttles because the macrocycle does not interact with the two stoppers. However, the active group, propargyloxyl, is introduced onto the two sides of the ring so that the rotaxane has the potential to be functionalized by further decoration.

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