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Benzoyl chloride, 4-chloro-3-fluoro(9CI), is a chemical compound characterized by the molecular formula C7H9ClFO. It is a clear, colorless to light yellow liquid with a pungent, irritating odor. Benzoyl chloride, 4-chloro-3-fluoro(9CI) is highly reactive and is commonly used as a key building block in the synthesis of various active pharmaceutical ingredients, including anti-inflammatory drugs and antibiotics. Additionally, it serves as a chemical intermediate in the production of agrochemicals, dyes, and fragrances. Due to its reactivity, it requires careful handling and storage to prevent irritation to the eyes, skin, and respiratory system, as well as to avoid potential hazards.

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  • 177787-25-6 Structure
  • Basic information

    1. Product Name: Benzoyl chloride, 4-chloro-3-fluoro- (9CI)
    2. Synonyms: Benzoyl chloride, 4-chloro-3-fluoro- (9CI);4-Chloro-3-fluorobenzoyl chloride 97%;3-Fluoro-4-chlorobenzoyl chloride;4-Chloro-3-fluorobenzoylchloride97%
    3. CAS NO:177787-25-6
    4. Molecular Formula: C7H3Cl2FO
    5. Molecular Weight: 193.0025232
    6. EINECS: N/A
    7. Product Categories: ACIDHALIDE
    8. Mol File: 177787-25-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 222℃
    3. Flash Point: 88℃
    4. Appearance: /
    5. Density: 1.462
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzoyl chloride, 4-chloro-3-fluoro- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoyl chloride, 4-chloro-3-fluoro- (9CI)(177787-25-6)
    11. EPA Substance Registry System: Benzoyl chloride, 4-chloro-3-fluoro- (9CI)(177787-25-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: CORROSIVE
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 177787-25-6(Hazardous Substances Data)

177787-25-6 Usage

Uses

Used in Pharmaceutical Industry:
Benzoyl chloride, 4-chloro-3-fluoro(9CI) is used as a key building block for the synthesis of various active pharmaceutical ingredients. It plays a crucial role in the development of anti-inflammatory drugs and antibiotics, contributing to the treatment and management of various health conditions.
Used in Agrochemical Production:
Benzoyl chloride, 4-chloro-3-fluoro(9CI) is utilized as a chemical intermediate in the production of agrochemicals, which are essential for enhancing crop productivity and protecting plants from pests and diseases.
Used in Dye and Fragrance Industries:
Benzoyl chloride, 4-chloro-3-fluoro(9CI) is also employed in the synthesis of dyes and fragrances, contributing to the vibrant colors and appealing scents in various consumer products.
Safety Precautions:
Due to its highly reactive nature, Benzoyl chloride, 4-chloro-3-fluoro(9CI) should be handled with caution to prevent irritation to the eyes, skin, and respiratory system. It is essential to follow proper safety measures during storage and handling to minimize the risk of accidental exposure and potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 177787-25-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,7,8 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 177787-25:
(8*1)+(7*7)+(6*7)+(5*7)+(4*8)+(3*7)+(2*2)+(1*5)=196
196 % 10 = 6
So 177787-25-6 is a valid CAS Registry Number.

177787-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-3-fluorobenzoyl chloride

1.2 Other means of identification

Product number -
Other names JRD-1336

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:177787-25-6 SDS

177787-25-6Upstream product

177787-25-6Relevant articles and documents

Novel hetero-cyclic compound and organic light emitting device comprising the same

-

Paragraph 0147-0150, (2019/02/26)

The present invention relates to a novel heterocyclic compound, which is capable of increasing efficiency and lifetime in an organic light emitting device, and an organic light emitting device using the same. The novel heterocyclic compound is represented

Design, synthesis, structure-activity relationships study and X-ray crystallography of 3-substituted-indolin-2-one-5-carboxamide derivatives as PAK4 inhibitors

Guo, Jing,Zhao, Fan,Yin, Wenbo,Zhu, Mingyue,Hao, Chenzhou,Pang, Yu,Wu, Tianxiao,Wang, Jian,Zhao, Dongmei,Li, Haitao,Cheng, Maosheng

, p. 197 - 209 (2018/06/12)

We have previously described the identification of indolin-2-one-5-carboxamides as potent PAK4 inhibitors. This study expands the structure-activity relationships on our original series by presenting several modifications in the lead compounds, 2 and 3. A series of novel derivatives was designed, synthesized, and evaluated in biochemical and cellular assay. Most of this series displayed nanomolar biochemical activity and potent antiproliferative activity against A549 and HCT116 cells. The representative compound 10a exhibited excellent enzyme inhibition (PAK4 IC50 = 25 nM) and cellular potency (A549 IC50 = 0.58 μM, HCT116 IC50 = 0.095 μM). An X-ray structure of compound 10a bound to PAK4 was obtained. Crystallographic analysis confirmed predictions from molecular modeling and helped refine SAR results. In addition, Compound 10a displayed focused multi-targeted kinase inhibition, good calculated drug-likeness properties. Further profiling of compound 10a revealed it showed weak inhibitory activity against various isoforms of human cytochrome P450.

N -pyridyl and pyrimidine benzamides as KCNQ2/Q3 potassium channel openers for the treatment of epilepsy

Amato, George,Roeloffs, Rosemarie,Rigdon, Greg C.,Antonio, Brett,Mersch, Theresa,McNaughton-Smith, Grant,Wickenden, Alan D.,Fritch, Paul,Suto, Mark J.

supporting information; experimental part, p. 481 - 484 (2011/08/22)

A series of N-pyridyl benzamide KCNQ2/Q3 potassium channel openers were identified and found to be active in animal models of epilepsy and pain. The best compound 12 [ICA-027243, N-(6-chloro-pyridin-3-yl)-3,4-difluoro-benzamide] has an EC50 of 0.38 μM and is selective for KCNQ2/Q3 channels. This compound was active in several rodent models of epilepsy and pain but upon repeated dosing had a number of unacceptable toxicities that prevented further development. On the basis of the structure-activity relationships developed around 12, a second compound, 51, [N-(2-chloro-pyrimidin-5-yl)-3,4-difluoro- benzamide, ICA-069673], was prepared and advanced into a phase 1 clinical study. Herein, we describe the structure-activity relationships that led to the identification of compound 12 and to the corresponding pyrimidine 51.

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