94135-19-0 Usage
General Description
2,6-dimethylbenzene-1,3,5-triamine, also known as m-xylylenediamine, is an organic compound with the chemical formula C8H12N2. It is a colorless solid that is soluble in water and polar organic solvents. It is commonly used in the production of various polymers, including nylon, polyurethane, and epoxy resins, where it acts as a crosslinking agent. It is also used as a curing agent for epoxy resins and as a corrosion inhibitor. 2,6-dimethylbenzene-1,3,5-triamine is considered to be moderately toxic, with potential adverse effects on the respiratory and central nervous systems. It is important for users to take appropriate safety precautions when handling this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 94135-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,3 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94135-19:
(7*9)+(6*4)+(5*1)+(4*3)+(3*5)+(2*1)+(1*9)=130
130 % 10 = 0
So 94135-19-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H13N3/c1-4-6(9)3-7(10)5(2)8(4)11/h3H,9-11H2,1-2H3
94135-19-0Relevant articles and documents
Synthesis and biological activity of flavanone derivatives
Shi, Lei,Feng, Xiu E,Cui, Jing Rong,Fang, Lian Hua,Du, Guan Hua,Li, Qing Shan
scheme or table, p. 5466 - 5468 (2011/01/03)
A series of new flavanone derivatives of farrerol was synthesized by a convenient method. The in vitro anti-tumor activity of these compounds was evaluated against human Bel-7402, HL-60, BGC-823 and KB cell lines, the protein tyrosine kinase (PTK) inhibitor activity was also tested. Their cytoprotective activity was tested using hydrogen peroxide (H2O2)-induced injury in human umbilical vein endothelial cells. Their in vitro anti-atherosclerosis activity was tested on vascular smooth muscle cells by the MTT method using tetrandrine as a positive contrast drug. The structures of all compounds synthesized were confirmed by 1H, 13C NMR and ESI-MS. Most of the compounds exhibited good pharmacological activity and the preliminary structure-activity relationships were described.
