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1-Phenyl-5-(trifluoromethyl)pyrazole-4-carbonyl chloride is a specific organofluorine chemical compound characterized by a pyrazole ring, which is an unsaturated five-member loop consisting of four carbon atoms and two nitrogen atoms. This ring is further substituted with a phenyl group and a carbonyl chloride group. Due to its unique chemical structure, it can engage in a variety of chemical reactions and is potentially utilized as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. Its properties and potential hazards are typically assessed through specific material safety data sheets.

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  • 175137-14-1 Structure
  • Basic information

    1. Product Name: 1-PHENYL-5-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE
    2. Synonyms: 1-PHENYL-5-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE;1-PHENYL-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBONYL CHLORIDE;1-Phenyl-5-(trifluoromethyl)pyrazole-4-carbonyl chloride 97%;1-Phenyl-5-(trifluoromethyl)pyrazole-4-carbonylchloride97%;1-Phenyl-5-(trifluoromethyl)pyrazole-4-carbonyl;1-Phenyl-5-(trifluoromethyl)-1H-pyrazole-4-carbonyl chloride 97%;1-Phenyl-5-(trifluoromethyl)-1H-pyrazole-4-carbonylchloride97%;TIMTEC-BB SBB001093
    3. CAS NO:175137-14-1
    4. Molecular Formula: C11H6ClF3N2O
    5. Molecular Weight: 274.63
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 175137-14-1.mol
  • Chemical Properties

    1. Melting Point: 40 °C
    2. Boiling Point: 110 °C
    3. Flash Point: 175.3°C
    4. Appearance: /
    5. Density: 1.55g/cm3
    6. Vapor Pressure: 8.13E-05mmHg at 25°C
    7. Refractive Index: 1.556
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-PHENYL-5-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-PHENYL-5-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE(175137-14-1)
    12. EPA Substance Registry System: 1-PHENYL-5-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE(175137-14-1)
  • Safety Data

    1. Hazard Codes: Xi,C
    2. Statements: 34
    3. Safety Statements: 26-36/37/39
    4. RIDADR: 3265
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: CORROSIVE
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 175137-14-1(Hazardous Substances Data)

175137-14-1 Usage

Uses

Used in Pharmaceutical Industry:
1-Phenyl-5-(trifluoromethyl)pyrazole-4-carbonyl chloride is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to participate in multiple chemical reactions, making it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, 1-Phenyl-5-(trifluoromethyl)pyrazole-4-carbonyl chloride is used as a building block in the creation of agrochemical products. Its reactivity and stability contribute to the formulation of effective pesticides and other agricultural chemicals.
Used in Dye Industry:
1-Phenyl-5-(trifluoromethyl)pyrazole-4-carbonyl chloride is employed as a key intermediate in the production of dyes. Its chemical properties enable the creation of a wide range of colorants used in various applications, such as textiles, plastics, and printing inks.

Check Digit Verification of cas no

The CAS Registry Mumber 175137-14-1 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 175137-14:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*7)+(2*1)+(1*4)=131
131 % 10 = 1
So 175137-14-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H6ClF3N2O/c12-10(18)8-6-16-17(9(8)11(13,14)15)7-4-2-1-3-5-7/h1-6H

175137-14-1SDS

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 1-PHENYL-5-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBONYL CHLORIDE

1.2 Other means of identification

Product number -
Other names 1-phenyl-5-(trifluoromethyl)-1H-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:175137-14-1 SDS

175137-14-1Relevant 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

Aromatic imide compounds and preparation method and application thereof

-

, (2016/10/09)

The invention discloses aromatic imide derivatives with the chemical structure shown as the general formula (I) and a preparation method and anticancer activity thereof. R1 and R2 are defined in the specification. Part of the compounds have good anticance

SPHINGOSINE-1-PHOSPHATE RECEPTOR AGONISTS

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Page/Page column 163, (2011/02/24)

Disclosed are compounds of Formula (I), or a stereoisomer or a pharmaceutically acceptable salt thereof, wherein: A is formula (II) Q is a substituted 5-membered monocyclic heteroaryl group; W is CH2, O, or NH; and R1, R2, R3, R4, R5, R6, m, n, t, and x are defined herein. Also disclosed are methods of using such compounds as selective agonists for G protein-coupled receptor S1P1, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.

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