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N-benzyl-N-[4-(benzylamino)-6-chloro-1,3,5-triazin-2-yl]amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30355-04-5

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30355-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30355-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,5 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30355-04:
(7*3)+(6*0)+(5*3)+(4*5)+(3*5)+(2*0)+(1*4)=75
75 % 10 = 5
So 30355-04-5 is a valid CAS Registry Number.

30355-04-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N,2-N-dibenzyl-6-chloro-1,3,5-triazine-2,4-diamine

1.2 Other means of identification

Product number -
Other names 2-Chlor-4.6-bis-benzylamino-s-triazin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30355-04-5 SDS

30355-04-5Downstream Products

30355-04-5Relevant academic research and scientific papers

Synthesis and antitumor evaluation of a novel series of triaminotriazine derivatives

Zheng, Mingfang,Xu, Chenghui,Ma, Jianwei,Sun, Yan,Du, Feifei,Liu, Hong,Lin, Liping,Li, Chuan,Ding, Jian,Chen, Kaixian,Jiang, Hualiang

, p. 1815 - 1827 (2008/02/03)

A series of triaminotriazine derivatives (compounds 5a-f, 6a-x, and 7a-g) was designed, synthesized, and evaluated for their inhibition activities to colorectal cancer (CRC) cell lines (HCT-116 and HT-29). Most of the synthesized compounds demonstrated moderate anti-proliferatory effects on both HCT-116 and HT-29 cell lines at the concentration of 10 μM. The inhibitory activities against HCT-116 and HT-29 cell lines were discussed to develop the structure-activity relationships of this new series. Compounds 6l and 6o exhibited prominent inhibition activities toward HCT-116, with IC50s of 0.76 and 0.92 μM, respectively. The in vivo antitumor studies and pharmacokinetics of compound 6l showed that it might be a promising new hit for further development of antitumor agents.

Synthesis of Macrocyclic, Triazine-Based Receptor Molecules

Loewik, Dennis W. P. M.,Lowe, Christopher R.

, p. 2825 - 2840 (2007/10/03)

The synthesis of triazine-based macrocyclic scaffolds is presented. The strategy employed allows for the facile functionalization of the macrocyclic molecules and combinatorial construction of putative receptor molecules. It is shown that the functional groups on the macrocyclic molecules, the size of the rings and the nature of the diamines linking the triazines can all be varied. In addition to the description of the stepwise synthesis of these compounds, it is shown that macrocycles based on triazine and xylenediamine are able to bind pyranosides and cyanuric acid.

Synthesis and biological evaluation of some new 3,4-dihydropyrimidin-4-ones

Modha, Jayesh,Datta, Neela,Parekh, Hansa

, p. 641 - 646 (2007/10/03)

Condensation of 5-cyano-2-hydrazino-3-N-methyl-6-phenyl/p-chlorophenyl-3,4-dihydropyrimidin-4 -one (3a and 3b) with 2,4-bisalkyl/arylamino-6-chloro-s-triazine (4) gave the corresponding 2,4-bisalkyl/arylamino-6-[5′-cyano-3′-N-methyl]-6′-phenyl/p -chlorophenyl-3′,4′-dihydropyrimidin-4′-one-2′-yl-hyd razino-s-triazines (5a-n and 6a-n). The compounds 4 have been prepared by the condensation of cyanuric chloride and different alkyl/aryl amines. The reaction between 5-cyano-3-N-methyl-2-methylthio-6-phenyl/p-chlorophenyl-3,4-dihydropyrimidin- 4-one (2a and 2b) with hydrazine hydrate furnished 3a and 3b, respectively. The condensation of 6-phenyl/p-chlorophenyl/5-cyano-2-mercapto-3,4-dihydropyrimidin-4-one (1a and 1b) with methyl iodide yielded 2a and 2b, respectively. All the products have been evaluated in vitro for their antimicrobial activity against several microbes and antitubercular activity against Mycobacterium tuberculosis H37 Rv. Copyright

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