Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2978-79-2

Post Buying Request

2978-79-2 Suppliers

Recommended suppliersmore

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

2978-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2978-79-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2978-79:
(6*2)+(5*9)+(4*7)+(3*8)+(2*7)+(1*9)=132
132 % 10 = 2
So 2978-79-2 is a valid CAS Registry Number.

2978-79-2Relevant articles and documents

A Kinetic Study on the Chemiluminescence of 9-Alkylacridines upon Air Oxidation in Alkaline Aprotic Solvents

Kamiya, Isao,Sugimoto, Takashi,Yamabe, Kuniaki

, p. 1735 - 1739 (1984)

9-Methyl- (1a), 9-benzyl- (1b), 9-(diphenylmethyl)- (1c), and 9-ethylacridine (1d) were employed to obtain luminescent features of the acridines.The decay of chemiluminescence (CL) exhibits a pseudo-first order behavior with apparent rate constants 0.10,

SYNTHESIS OF SUBSTITUTED ACRIDINES

-

, (2018/12/13)

Disclosed is a method of making substituted acridines. The method includes the step of reacting a bis(halophenyl) amine with an alkyne for a time and at a temperature to yield a substituted acridine.

Lattice energetics and thermochemistry of acridine derivatives and substituted acridinium trifluoromethanesulphonates

Zadykowicz, Beata,Storoniak, Piotr

, p. 1613 - 1624 (2017/08/16)

The enthalpies and temperatures of melting of eight 9-substituted acridines (alkyl, aryl or alkoxy) (I) and six their 10-methylated-acridinium trifluoromethanesulphonate (II) derivatives were measured by DSC. The enthalpies and temperatures of volatilisation of the first group of compounds were also determined by DSC or obtained by fitting TG curves to the Clausius–Clapeyron relationship. By combining the enthalpies of formation of gaseous acridines or 10-methylacridinium trifluoromethanesulphonate ions, obtained by the DFT method, and the corresponding enthalpies of sublimation and/or crystal lattice enthalpies, the enthalpies of formation of the compounds in the solid phase were predicted. For compounds whose crystal structures are known, experimental enthalpies of sublimation correspond reasonably well to crystal lattice enthalpies predicted theoretically as the sum of electrostatic, dispersive and repulsive interactions. Analysis of crystal lattice enthalpy contributions indicates that dispersive interactions between molecules always predominate in the case of acridine derivatives, whilst the crystal lattices of their quaternary salts are stabilised by electrostatic interactions between ions. Only in the case of 9-bromomethylacridine derivative, which crystallises in the monohydrated form, electrostatic contribution to the crystal lattice energy is significantly higher than in the other investigated acridines.

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

What can I do for you?
Get Best Price

Get Best Price for 2978-79-2