Welcome to LookChem.com Sign In|Join Free
  • or
1,3-Propanediamine, N,N'-bis(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133545-35-4

Post Buying Request

133545-35-4 Suppliers

Recommended suppliers

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

133545-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133545-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,4 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 133545-35:
(8*1)+(7*3)+(6*3)+(5*5)+(4*4)+(3*5)+(2*3)+(1*5)=114
114 % 10 = 4
So 133545-35-4 is a valid CAS Registry Number.

133545-35-4Relevant academic research and scientific papers

Catalyst-Free Synthesis of Aryl Diamines via a Three-Step Reaction Process

Bulut, Safak,Queen, Wendy L.

, p. 3806 - 3818 (2018/04/14)

The formation of C-N bonds with aryl amines is one of the most widely studied reactions in organic chemistry. Despite this, it is still highly challenging, often requiring expensive, precious metal-based catalysts. Here we report an easy catalyst-free methodology for constructing C-N bonds. The method, which proceeds via the in situ formation of closed ring amidinium ions, allows the preparation of a series of symmetrical and/or unsymmetrical aryl diamines in notably high yields (82-98%) and purity and with a variety of different substituents. The methodology is shown successful for the preparation of aryl diamines having para- and/or meta-substituted carboxyl, nitro, bromo, methoxy, or methyl groups. This green synthetic pathway, which is catalyst free, requires only three steps, and proceeds without the need for purification. Further, it is a new sustainable, economically viable method to achieve an otherwise challenging bond formation.

Bis-4-aminobenzamidines: Versatile, fluorogenic A/T-selective dsDNA binders

Vazquez, Olalla,Sanchez, Mateo I.,Martinez-Costas, Jose,Vazquez, M. Eugenlo,Mascarenas, Jose L.

supporting information; experimental part, p. 216 - 219 (2010/03/30)

(Figure presented) N1, N3-Bls(4-amldlnophenyl) propane-1, 3-dlamlne (BAPPA, R = H) Is a blsamlnobenzamldlne fluorogenlc derivative that displays a large Increase In Its emission fluorescence when bound to the minor groove of specific A/T DNA sites (Kd for an AATT site ~ 79 ± 6 nM). Moreover, the structural characteristics of BAPPA allow the easy Introduction of functional groups that protrude out of the DNA surface.

Double secondary para-phenylenediamine compounds, dye compositions comprising same, and dyeing process using the compositions

-

Page/Page column 6-7, (2008/06/13)

The present disclosure relates to double secondary para-phenylenediamine dye compounds. The present disclosure further relates to a dye composition comprising at least one double secondary para-phenylenediamine compound, a process for dyeing keratin fiber

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 133545-35-4