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| Synonyms | 4-chloro benzoyl chloride | 4-Chlorobenzoylchloride | 4-chlorobenzoyl-chloride | MFCD00000686 | 4-Chlorobenzoyl vhloride | DTXSID4051619 | 4-chloro benzoylchloride | p-chloro benzoylchloride | DTXCID9030171 | EC 204-515-3 | p-Chlorobenzoyl chloride | p-ch |
|---|---|
| Specifications & Purity | ≥98%(GC) |
| Storage Temp | Argon charged |
| Shipped In | Normal |
| Product Description |
4-Chlorobenzoyl chloride was used to synthesize 4-chlorobenzoyl CoA by reacting it with CoA in KHCO3 buffer. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Halobenzoic acids and derivatives |
| Direct Parent | 4-halobenzoic acids and derivatives |
| Alternative Parents | Benzoyl derivatives Chlorobenzenes Aryl chlorides Acyl chlorides Organooxygen compounds Organochlorides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | 4-halobenzoic acid or derivatives - Benzoyl - Halobenzene - Chlorobenzene - Aryl halide - Aryl chloride - Acyl halide - Acyl chloride - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as 4-halobenzoic acids and derivatives. These are benzoic acids or derivatives carrying a halogen atom at the 4-position of the benzene ring. |
| External Descriptors | monochlorobenzenes - acyl chloride |
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| Pubchem Sid | 504751695 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751695 |
| IUPAC Name | 4-chlorobenzoyl chloride |
| INCHI | InChI=1S/C7H4Cl2O/c8-6-3-1-5(2-4-6)7(9)10/h1-4H |
| InChIKey | RKIDDEGICSMIJA-UHFFFAOYSA-N |
| Smiles | C1=CC(=CC=C1C(=O)Cl)Cl |
| Isomeric SMILES | C1=CC(=CC=C1C(=O)Cl)Cl |
| WGK Germany | 1 |
| RTECS | DM6635510 |
| UN Number | 3265 |
| Molecular Weight | 175.01 |
| Beilstein | 471606 |
| Reaxy-Rn | 471606 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=471606&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jul 09, 2025 | C106079 | |
| Certificate of Analysis | Feb 28, 2025 | C106079 | |
| Certificate of Analysis | Feb 28, 2025 | C106079 | |
| Certificate of Analysis | Dec 17, 2024 | C106079 | |
| Certificate of Analysis | Dec 17, 2024 | C106079 | |
| Certificate of Analysis | Dec 17, 2024 | C106079 | |
| Certificate of Analysis | Nov 08, 2023 | C106079 | |
| Certificate of Analysis | May 11, 2023 | C106079 | |
| Certificate of Analysis | May 11, 2023 | C106079 | |
| Certificate of Analysis | May 11, 2023 | C106079 | |
| Certificate of Analysis | Nov 11, 2022 | C106079 | |
| Certificate of Analysis | Nov 11, 2022 | C106079 | |
| Certificate of Analysis | Dec 24, 2021 | C106079 | |
| Certificate of Analysis | Dec 24, 2021 | C106079 | |
| Certificate of Analysis | Dec 24, 2021 | C106079 |
| Solubility | Soluble in Toluene, ethanol, ether, acetone, and hydrolyses in water. |
|---|---|
| Sensitivity | Moisture Sensitive |
| Refractive Index | 1.5756 |
| Flash Point(°F) | 221 °F |
| Flash Point(°C) | 105℃ |
| Boil Point(°C) | 222°C |
| Melt Point(°C) | 12°C |
| Molecular Weight | 175.010 g/mol |
| XLogP3 | 3.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 173.964 Da |
| Monoisotopic Mass | 173.964 Da |
| Topological Polar Surface Area | 17.100 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 128.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
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| 1. Zhongda Wu, Yanting Du, Quan Zhou, Lianqing Chen. (2020) One pot solvothermal synthesis of novel fluorescent phloem-mobile phenylpyrazole amide pesticides fused olefin moieties to enhance insecticidal bioactivities and photodegradation properties. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 163 (51). |
| 2. Shengli Cheng, Zhihuan Weng, Xin Wang, Yunxing Pan, Xigao Jian, Jinyan Wang. (2017) Oxidative protection of carbon fibers with carborane-containing polymer. CORROSION SCIENCE, 127 (59). |