Welcome to LookChem.com Sign In|Join Free
  • or
Benzenamine, 4-(5-chloro-1H-tetrazol-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14210-33-4

Post Buying Request

14210-33-4 Suppliers

Recommended suppliers

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

14210-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14210-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14210-33:
(7*1)+(6*4)+(5*2)+(4*1)+(3*0)+(2*3)+(1*3)=54
54 % 10 = 4
So 14210-33-4 is a valid CAS Registry Number.

14210-33-4Relevant academic research and scientific papers

Preparation and characterization of novel side-chain azobenzene polymers containing tetrazole group

Xue, Xiaoqiang,Yang, Jing,Huang, Wenyan,Yang, Hongjun,Jiang, Bibiao

, p. 61 - 70 (2015/10/19)

A novel methacrylate monomer containing azobenzene chromophore and tetrazole moiety, 4′-(2-methacryloxyethyl)methylamino-4-(5-chlorotetrazol-1-yl)azobenzene (MACA), was synthesized and polymerized to form homopolymer (PMACA) via reversible addition-fragme

A kinetic investigation of the thermal rearrangement of allyloxytetrazoles to N-allyltetrazolones

Cristiano, M. Lurdes S.,Johnstone, Robert A. W.

, p. 489 - 494 (2007/10/03)

The mechanism of the thermal rearrangement of 1-aryl-5-allyloxytetrazoles 1 to give 1-aryl-4-allyltetrazolones 2 in very high yield has been investigated through kinetic studies in one polar and one less polar solvent. The results suggest mainly a concerted [3,3] sigmatropic process, in which a partially positively charged allyl group migrates from oxygen to nitrogen, similar to the polar transition state found in the Claisen rearrangement.

Metal-assisted Reactions: Part 19. Burst Kinetics in Heterogeneous Catalytic Transfer Hydrogenolysis

Johnstone, Robert A. W.,Price, Peter J.

, p. 1069 - 1076 (2007/10/02)

Arene formation by catalytic transfer hydrogenolysis of aryloxytetrazolyl ethers in the liquid-phase shows biphasic concentration-time curves which indicate rate-limiting dissociation of heterogeneous complexes between catalyst and one of the reaction products, a tetrazolone.A dependence of catalytic reaction rate on pH and following modifications made to the catalyst are reported also.

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 14210-33-4