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N-[5-(TRIFLUOROMETHYL)PYRID-2-YL]-N-METHYLHYDRAZINE is a chemical compound characterized by the presence of fluorine and nitrogen-based functional groups. It has a molecular formula of C6H7F3N3, which signifies that it is composed of six carbon atoms, seven hydrogen atoms, three fluorine atoms, and three nitrogen atoms. N-[5-(TRIFLUOROMETHYL)PYRID-2-YL]-N-METHYLHYDRAZINE is a member of the hydrazine and derivatives category. The inclusion of a trifluoromethyl group imparts unique chemical properties to the molecule, which can be advantageous in certain chemical reactions. However, detailed information about its properties, applications, and safety measures is not extensively documented, suggesting that it may be utilized in specialized or industry-specific contexts.

163620-24-4

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163620-24-4 Usage

Uses

Used in Chemical Synthesis:
N-[5-(TRIFLUOROMETHYL)PYRID-2-YL]-N-METHYLHYDRAZINE is used as a chemical intermediate for the synthesis of various complex molecules. Its unique trifluoromethyl group and hydrazine functionality make it a valuable building block in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
In the field of research and development, N-[5-(TRIFLUOROMETHYL)PYRID-2-YL]-N-METHYLHYDRAZINE is employed as a reagent in the exploration of new chemical reactions and processes. Its distinct properties can lead to the discovery of novel reaction pathways and the development of innovative synthetic methods.
Used in Pharmaceutical Industry:
N-[5-(TRIFLUOROMETHYL)PYRID-2-YL]-N-METHYLHYDRAZINE is used as a key component in the development of new drugs. Its unique structure and reactivity can contribute to the creation of potential therapeutic agents, particularly in the areas of oncology, infectious diseases, and other medical conditions where novel treatments are needed.
Used in Agrochemical Industry:
In the agrochemical sector, N-[5-(TRIFLUOROMETHYL)PYRID-2-YL]-N-METHYLHYDRAZINE is utilized as a starting material for the synthesis of new pesticides and herbicides. Its chemical properties can be harnessed to develop more effective and environmentally friendly agricultural products.
Used in Material Science:
N-[5-(TRIFLUOROMETHYL)PYRID-2-YL]-N-METHYLHYDRAZINE is used as a precursor in the development of advanced materials, such as polymers and composites, with tailored properties. Its incorporation into these materials can lead to improved performance characteristics, such as enhanced stability, durability, and functionality.

Check Digit Verification of cas no

The CAS Registry Mumber 163620-24-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,6,2 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 163620-24:
(8*1)+(7*6)+(6*3)+(5*6)+(4*2)+(3*0)+(2*2)+(1*4)=114
114 % 10 = 4
So 163620-24-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H12ClN3/c12-8-1-2-9-10(15-6-4-13)3-5-14-11(9)7-8/h1-3,5,7H,4,6,13H2,(H,14,15)

163620-24-4 Well-known Company Product Price

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  • Aldrich

  • (L510416)  2-Hydrazinyl-5-trifluoromethylpyridine  AldrichCPR

  • 163620-24-4

  • L510416-1G

  • 514.80CNY

  • Detail

163620-24-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-1-[5-(trifluoromethyl)pyridin-2-yl]hydrazine

1.2 Other means of identification

Product number -
Other names 2-(1-methylhydrazino)-5-(trifluoromethyl)pyridine

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:163620-24-4 SDS

163620-24-4Downstream Products

163620-24-4Relevant articles and documents

Photochromic compounds

-

, (2008/06/13)

A spiro (indolino) oxazine compound of general formula (I) STR1 wherein R1 represents a group of the formula --NR2 R3 wherein each of R2 and R3, which may be the same or different, independently represents an alkyl group, or a carbocyclic group, preferably aryl, or a heterocyclic group, or R2 and R3 taken together with the nitrogen atom to which they are attached represent a heterocyclic ring having one or more heteroatoms and which may optionally carry at least one substituent selected from alkyl, aryl or heteroaryl groups; --X-- is selected from --O--, --S--, --Se--, --NH-- or --NR-- wherein R represents an alkyl group, and ring A is a carbocyclic or heterocyclic ring which can be optionally substituted with a group of formula R8 as defined above, or may optionally have a carbocyclic or heterocyclic ring fused thereto; and wherein R4 -R8 are as defined in the specification. The spiro (indolino) oxazine compounds of the invention are useful as photochromic materials.

Red colouring photochromic 6′-substituted spiroindolinonaphth[2,1-b][1,4]oxazines

Rickwood,Marsden,Ormsby,Staunton,Wood,Hepworth,Gabbutt

, p. 17 - 24 (2007/10/02)

Electron donating/withdrawing substituents and electronegative centres have been successfully employed in substantially widening the range of photo-generated colours available in the spiroindolinonaphthoxazine class of photochromic materials.

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