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2,3-bis(benzyloxy)-N-(3-hydroxypropyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

705281-82-9

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705281-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 705281-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,5,2,8 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 705281-82:
(8*7)+(7*0)+(6*5)+(5*2)+(4*8)+(3*1)+(2*8)+(1*2)=149
149 % 10 = 9
So 705281-82-9 is a valid CAS Registry Number.

705281-82-9Downstream Products

705281-82-9Relevant academic research and scientific papers

Hexadentate β-Dicarbonyl(bis-catecholamine) Ligands for Efficient Uranyl Cation Decorporation: Thermodynamic and Antioxidant Activity Studies

Zhang, Qingchun,Jin, Bo,Zheng, Tian,Tang, Xingyan,Guo, Zhicheng,Peng, Rufang

, p. 14626 - 14634 (2019)

The special linear dioxo cation structure of the uranyl cation, which relegates ligand coordination to an equatorial plane perpendicular to the O=U=O vector, poses an unusual challenge for the rational design of efficient chelating agents. Therefore, the

Synthesis and characterization of a potential bifunctional C60-Ih fullerene-based catechol amide ligand

Zhang, Qingchun,Jin, Bo,Peng, Rufang,Lei, Shan,Chu, Shijin

, p. 204 - 206 (2015)

The new C60-Ih fullerene-based catechol amide derivatives C60{C[COO(CH2)nCAM]2} [n = 2, 3 or 4; CAM = 2,3-Ph(OH)2CONH] were prepared using a modified Bingel-type reaction of Csu

Symmetrical 1,3-dicarbonyl biscatecholamide ligands as sequestering agents for uranyl decorporation

Zhang, Qingchun,Jin, Bo,Peng, Rufang,Lei, Shan,Chu, Shijin

, p. 417 - 423 (2015/02/05)

The synthesis of a series of new symmetrical 1,3-dicarbonyl biscatecholamide ligands CH2[COX(CH2)nCAM; X = O, NH; n = 2, 3, 4]2 [CAM = 2,3-Ph(OH)2CONH] is presented. 1H NMR, 13C

Total Synthesis of Petrobactin and Its Homologues as Potential Growth Stimuli for Marinobacter hydrocarbonoclasticus, an Oil-Degrading Bacteria

Gardner, Richard Andrew,Kinkade, Rebecca,Wang, Chaojie,Phanstiel IV, Otto

, p. 3530 - 3537 (2007/10/03)

A modular synthesis was developed to access petrobactin, a catechol-containing siderophore isolated from Marinobacter hydrocarbonoclasticus. A range of petrobactin homologues with differing dihydroxybenzamide motifs and in one case an increased number of

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