Welcome to LookChem.com Sign In|Join Free
  • or
Guanidine, (2,4-dinitrophenyl)-, also known as 2,4-dinitrophenyl guanidine, is a chemical compound with the molecular formula C7H7N5O4. It is a derivative of guanidine, an organic compound containing a functional group with two nitrogen atoms and one carbon atom. The 2,4-dinitrophenyl group is attached to the guanidine, resulting in a yellow crystalline solid. Guanidine, (2,4-dinitrophenyl)- is primarily used as a reagent in various chemical analyses and as a precursor in the synthesis of other organic compounds. Due to its potential toxicity and reactivity, it is important to handle 2,4-dinitrophenyl guanidine with caution and proper safety measures.

951-66-6

Post Buying Request

951-66-6 Suppliers

Recommended suppliers

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

951-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 951-66-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 951-66:
(5*9)+(4*5)+(3*1)+(2*6)+(1*6)=86
86 % 10 = 6
So 951-66-6 is a valid CAS Registry Number.

951-66-6Downstream Products

951-66-6Relevant academic research and scientific papers

One-Pot Evolution of Ageladine A through a Bio-Inspired Cascade towards Selective Modulators of Neuronal Differentiation

Iwata, Takayuki,Otsuka, Satoshi,Tsubokura, Kazuki,Kurbangalieva, Almira,Arai, Daisuke,Fukase, Koichi,Nakao, Yoichi,Tanaka, Katsunori

supporting information, p. 14707 - 14716 (2016/10/03)

A bio-inspired cascade reaction has been developed for the construction of the marine natural product ageladine A and a de novo array of its N1-substituted derivatives. This cascade features a 2-aminoimidazole formation that is modeled after an arginine post-translational modification and an aza-electrocyclization. It can be effectively carried out in a one-pot procedure from simple anilines or guanidines, leading to structural analogues of ageladine A that had been otherwise synthetically inaccessible. We found that some compounds out of this structurally novel library show a significant activity in modulating the neural differentiation. Namely, these compounds selectively activate or inhibit the differentiation of neural stem cells to neurons, while being negligible in the differentiation to astrocytes. This study represents a successful case in which the native biofunction of a natural product could be altered by structural modifications.

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 951-66-6