735255-56-8 Usage
General Description
(4-Chloro-pyridin-2-yl)-dimethyl-amine is a chemical compound with the molecular formula C7H9ClN2. It is an organic compound with a chloro-substituted pyridine ring and a dimethylamine group. (4-CHLORO-PYRIDIN-2-YL)-DIMETHYL-AMINE is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a reagent in chemical reactions and as a catalyst in organic synthesis. The chemical properties of (4-chloro-pyridin-2-yl)-dimethyl-amine make it a valuable and versatile intermediate in the production of a wide range of products for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 735255-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,5,2,5 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 735255-56:
(8*7)+(7*3)+(6*5)+(5*2)+(4*5)+(3*5)+(2*5)+(1*6)=168
168 % 10 = 8
So 735255-56-8 is a valid CAS Registry Number.
735255-56-8Relevant articles and documents
Nucleophilic Aromatic Substitution Reactions in Water Enabled by Micellar Catalysis
Isley, Nicholas A.,Linstadt, Roscoe T. H.,Kelly, Sean M.,Gallou, Fabrice,Lipshutz, Bruce H.
supporting information, p. 4734 - 4737 (2015/10/12)
Given the huge dependence on dipolar, aprotic solvents such as DMF, DMSO, DMAc, and NMP in nucleophilic aromatic substitution reactions (SNAr), a simple and environmentally friendly alternative is reported. Use of a "benign-by-design" nonionic surfactant, TPGS-750-M, in water enables nitrogen, oxygen, and sulfur nucleophiles to participate in SNAr reactions. Aromatic and heteroaromatic substrates readily participate in this micellar catalysis, which takes place at or near ambient temperatures.
