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4-Trifluoromethyl-2,6-pyridinediamine is a chemical compound with the molecular formula C7H7F3N4. It is characterized by the presence of a pyridine ring, a six-membered aromatic ring with one nitrogen atom, which is substituted by a trifluoromethyl group and two amino groups at the 2nd and 6th positions. 4-trifluoromethyl-2,6-pyridinediamine falls under the category of organic compounds, specifically those featuring fluorine. It is relatively less common and thus, less well-studied than other chemicals. Its properties like solubility, toxicity, and reactivity are largely unknown and would likely depend on its specific molecular interactions. As with all chemicals, proper precautions should be taken while handling 4-trifluoromethyl-2,6-pyridinediamine.

130171-52-7

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130171-52-7 Usage

Uses

Since the provided materials do not specify the uses of 4-trifluoromethyl-2,6-pyridinediamine, it is not possible to list its applications based on the given information. However, based on its chemical structure, it can be inferred that it may have potential applications in various fields such as pharmaceuticals, materials science, or as an intermediate in the synthesis of other compounds. Further research and experimentation would be required to determine its specific uses and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 130171-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,7 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 130171-52:
(8*1)+(7*3)+(6*0)+(5*1)+(4*7)+(3*1)+(2*5)+(1*2)=77
77 % 10 = 7
So 130171-52-7 is a valid CAS Registry Number.

130171-52-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(trifluoromethyl)pyridine-2,6-diamine

1.2 Other means of identification

Product number -
Other names 4-trifluoromethyl-pyridine-2,6-diamine

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:130171-52-7 SDS

130171-52-7Downstream Products

130171-52-7Relevant academic research and scientific papers

METHOD FOR PRODUCING 2-AMINO-4-(TRIFLUOROMETHYL)PYRIDINE

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Page/Page column 6-7, (2012/12/13)

The present invention relates to a process for producing a 2-amino-4-trifluoromethylpyridine. Specifically, the present invention provides a process for producing a compound represented by the formula (I) or a salt thereof: (in the formula, X1 is the same as X1 in the formula (II) below), which includes allowing a compound represented by the formula (II): (in the formula, each of X1 and X2 is independently a chlorine atom or a bromine atom) to react with ammonia in the presence of a hydrophilic ether; and also a process for producing 2-amino-4-trifluoromethyl pyridine or a salt thereof, which comprises subjecting the compound of the formula (I) as produced by the foregoing process to dehalogenation,

Orally active aminopyridines as inhibitors of tetrameric fructose-1,6-bisphosphatase

Hebeisen, Paul,Haap, Wolfgang,Kuhn, Bernd,Mohr, Peter,Wessel, Hans Peter,Zutter, Ulrich,Kirchner, Stephan,Ruf, Armin,Benz, J?rg,Joseph, Catherine,Alvarez-Sánchez, Rubén,Gubler, Marcel,Schott, Brigitte,Benardeau, Agnes,Tozzo, Effie,Kitas, Eric

scheme or table, p. 3237 - 3242 (2011/07/07)

A novel sulfonylureido pyridine series exemplified by compound 19 yielded potent inhibitors of FBPase showing significant glucose reduction and modest glycogen lowering in the acute db/db mouse model for Type-2 diabetes. Our inhibitors occupy the allosteric binding site and also extend into the dyad interface region of tetrameric FBPase.

NEW PYRIDINES AS FBPASE INHIBITORS FOR TREATMENT OF DIABETES

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Page/Page column 30, (2009/06/27)

Compounds of formula (I) as well as pharmaceutically acceptable salts and esters thereof wherein the residues have the significance given in claim 1 and which can be used in the form of pharmaceutical compositions.

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