Welcome to LookChem.com Sign In|Join Free
  • or
C32H52N4O9 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1039115-89-3

Post Buying Request

1039115-89-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1039115-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1039115-89-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,9,1,1 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1039115-89:
(9*1)+(8*0)+(7*3)+(6*9)+(5*1)+(4*1)+(3*5)+(2*8)+(1*9)=133
133 % 10 = 3
So 1039115-89-3 is a valid CAS Registry Number.

1039115-89-3Upstream product

1039115-89-3Relevant academic research and scientific papers

Selective head-to-tail recognition in hydrazide-based molecular duplex strands induced by spectator secondary electrostatic interactions

Yang, Yong,Xiang, Jun-Feng,Xue, Min,Hu, Hai-Yu,Chen, Chuan-Feng

, p. 4198 - 4203 (2008)

Due to spectator secondary electrostatic interactions, nonsymmetric mono-Boc-mono-acetyl terminated hydrazide-based oligomers displayed a head-to-tail dimerization mode, which was evidenced by 1H NMR, and 2D NOESY experiments. Dynamic behavior of the molecular duplex strands was also explored by variable temperature 1H NMR experiments.

Supramolecular substitution reactions between hydrazide-based molecular duplex strands: Complexation induced nonsymmetry and dynamic behavior

Yang, Yong,Xiang, Jun-Feng,Xue, Min,Hu, Hai-Yu,Chen, Chuan-Feng

, p. 6369 - 6377 (2008/12/22)

(Chemical Equation Presented) Supramolecular substitution reactions between hydrazide-based oligomers 1a-c and 2a-c were systematically investigated. Each oligomer existed as hydrogen-bonding mediated molecular duplex strands or a polymeric zipper structure in apolar solvents. But when another oligomer with complementary hydrogen bonding sites was added, a heterodimer structure formed due to supramolecular substitution reaction driven by the formation of more hydrogen bonds, which was evidenced by NMR experiments, sometimes gel-sol transition. When a nonsymmetric oligomer and a symmetric oligomer were involved, complexation-induced nonsymmetry was observed. When two nonsymmetric oligomers were involved, two hydrogen-bonded isomers were observed in solution. Variable-temperature 1H NMR experiments further revealed unique dynamic behavior for the individual oligomer and the complexes. When diacetyl-terminated oligomer 1c was involved, slides perpendicular to hydrogen bonds between two constituent molecules were observed, which led to complicated 1H NMR spectra at lower temperature; otherwise, high selectivity was obtained. Combined with the results we reported previously, a detailed picture of the structure-property relationship for our hydrazide-based oligomers was depicted, which would provide guidelines for the design of hydrazide-based fine-tuning functional materials.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1039115-89-3