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CAS

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175137-19-6

2-(4-Chlorophenyl)-3-(trifluoromethyl)pyrazole-4-carbonyl chloride is a pyrazole derivative with the molecular formula C10H5ClF3N3O and a molecular weight of 265.6 g/mol. It features a reactive carbonyl chloride functional group and is known for its unique structure and reactivity. This chemical compound serves as a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatility in organic synthesis.

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  • 2-(4-chlorophenyl)-3-(trifluoromethyl)pyrazole-4-carbonyl chloride

    Cas No: 175137-19-6

  • USD $ 1.9-2.9 / Gram

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  • 175137-19-6 Structure

  • Basic information

    1. Product Name: 2-(4-CHLOROPHENYL)-3-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE
    2. Synonyms: BUTTPARK 46\18-27;2-(4-CHLOROPHENYL)-3-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE;1-(4-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBONYL CHLORIDE;TIMTEC-BB SBB001267;2-(4-Chlorophenyl)-3-(trifluoromethyl)pyrazole-4-carbonyl chloride 97%;2-(4-Chlorophenyl)-3-(trifluoromethyl)pyrazole-4-carbonylchloride97%;1-(4-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE;2-(4-CHLOROPHENYL)-3-(TRIFLUOROMETHYL) PYRAZOLE-N 4-CARBONYL CHLORIDE
    3. CAS NO:175137-19-6
    4. Molecular Formula: C11H5Cl2F3N2O
    5. Molecular Weight: 309.07
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 175137-19-6.mol

  • Chemical Properties

    1. Melting Point: 51 °C
    2. Boiling Point: 120 °C
    3. Flash Point: 252.5°C
    4. Appearance: /
    5. Density: 1.361g/cm3
    6. Vapor Pressure: 6.74E-10mmHg at 25°C
    7. Refractive Index: 1.662
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(4-CHLOROPHENYL)-3-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(4-CHLOROPHENYL)-3-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE(175137-19-6)
    12. EPA Substance Registry System: 2-(4-CHLOROPHENYL)-3-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE(175137-19-6)

  • Safety Data

    1. Hazard Codes: Xi,C
    2. Statements: 34
    3. Safety Statements: 26-36/37/39
    4. RIDADR: 3261
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: CORROSIVE
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 175137-19-6(Hazardous Substances Data)

175137-19-6 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-Chlorophenyl)-3-(trifluoromethyl)pyrazole-4-carbonyl chloride is used as a building block for the synthesis of pharmaceuticals. Its unique structure and reactivity allow for the creation of chemical compounds with diverse applications in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(4-Chlorophenyl)-3-(trifluoromethyl)pyrazole-4-carbonyl chloride is utilized as an intermediate for the preparation of various agrochemicals. Its role in organic synthesis contributes to the production of compounds that can be used in crop protection and other agricultural applications.
Safety Note:
It is crucial to handle 2-(4-Chlorophenyl)-3-(trifluoromethyl)pyrazole-4-carbonyl chloride with care, as it may pose hazards if not properly managed. Proper safety measures should be taken during its use to ensure the well-being of individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 175137-19-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 175137-19:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*7)+(2*1)+(1*9)=136
136 % 10 = 6
So 175137-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H9FN4/c11-7-3-1-6(2-4-7)8-5-9(12)15-10(13)14-8/h1-5H,(H4,12,13,14,15)

175137-19-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Chlorophenyl)-3-(trifluoromethyl)pyrazole-4-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 1-(4-chlorophenyl)-5-(trifluoromethyl)pyrazole-4-carbonyl chloride

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:175137-19-6 SDS

175137-19-6Relevant articles and documents

Synthesis, Biological Evaluation, and 3D-QSAR Studies of N-(Substituted pyridine-4-yl)-1-(substituted phenyl)-5-trifluoromethyl-1 H-pyrazole-4-carboxamide Derivatives as Potential Succinate Dehydrogenase Inhibitors

Wu, Zhibing,Park, Hyung-Yeon,Xie, Dewen,Yang, Jingxin,Hou, Shuaitao,Shahzad, Nasir,Kim, Chan Kyung,Yang, Song

, p. 1214 - 1223 (2021/02/06)

A series of new fungicides that can inhibit the succinate dehydrogenase (SDH) was classified and named as SDH inhibitors by the Fungicide Resistance Action Committee in 2009. To develop more potential SDH inhibitors, we designed and synthesized a novel se

Phenylpyrazole amide derivative as well as preparation method and application thereof

-

Paragraph 0026-0028, (2020/09/08)

The invention discloses a phenylpyrazole amide derivative as well as a preparation method and application thereof. The structure of the derivative is shown as a formula (I). The compound provided by the invention is simple and convenient in preparation me

Preparation and application of triazole heterocyclic compound containing heteroaryl amide structure

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Paragraph 0085; 0093; 0094, (2019/11/14)

The invention discloses a triazole heterocyclic compound containing a heteroaryl amide structure, a geometrical isomer of triazole heterocyclic compound containing the heteroaryl amide structure and pharmacologically acceptable salt, hydrate, solvate or p

Pyrazole-amides and sulfonamides as sodium channel modulators

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Page/Page column 12-13, (2010/02/10)

Compounds of the present invention modulate PN3 in mammals and are useful in treating pain in mammals.

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