| 4-Chlorobenzoyl chloride Basic information | Uses |
| 4-Chlorobenzoyl chloride Chemical Properties |
Melting point | 11-14 °C (lit.) | Boiling point | 102-104 °C/11 mmHg (lit.) | density | 1.365 g/mL at 20 °C (lit.) | vapor pressure | 5.8-73.9Pa at 20-50℃ | refractive index | n20/D 1.578(lit.) | Fp | 221 °F | storage temp. | Store below +30°C. | solubility | soluble in Chloroform, DMSO | form | Liquid | color | Clear colorless to faintly colored | explosive limit | 1.5-15%(V) | Water Solubility | Reacts with water. Reacts with alcohol. | FreezingPoint | 12~14℃ | Sensitive | Moisture Sensitive | BRN | 471606 | Stability: | Stable. Moisture sensitive. Incompatible with strong oxidizing agents. | LogP | 2.52 at 25℃ | CAS DataBase Reference | 122-01-0(CAS DataBase Reference) | NIST Chemistry Reference | 4-Chlorobenzoic acid chloride(122-01-0) | EPA Substance Registry System | Benzoyl chloride, 4-chloro- (122-01-0) |
Hazard Codes | C | Risk Statements | 34-36/37 | Safety Statements | 26-36/37/39-45-28A | RIDADR | UN 3265 8/PG 2 | WGK Germany | 1 | RTECS | DM6635510 | F | 10-19-21 | TSCA | Yes | HazardClass | 8 | PackingGroup | II | HS Code | 29163900 |
| 4-Chlorobenzoyl chloride Usage And Synthesis |
Uses | 4-Chlorobenzoyl Chloride is used as a promoter in the synthesis of α-aminonitriles. It is also used as a derivatization agent and self-assembling dipole molecule to improve hole injection in conjugated polymers. In addition. It is an important organic intermediate to synthetize substituted 4-chlorobenzoyl products.
| Chemical Properties | liquid | Uses | 4-Chlorobenzoyl chloride was used to synthesize 4-chlorobenzoyl CoA by reacting it with CoA in KHCO3 buffer. 4-Chlorobenzoyl chloride may be used in the following studies Acylation of benzene using different solid acid catalysts such as dodecatungstophosphoric acid (DTPA), DTPA/K-10 clay, K-10, Amberlite, Amberlyst-15, Indion-130, Filtrol-24 clay and sulfated zirconia, Preparation of 1-(4-chlorobenzoyl)-2, 7-dimethoxynaphthalene, Preparation of 4-chlorobenzoyl CoA, via reaction with CoA in KHCO3 buffer, Preparation of 1-aryloxyacetyl-4-(4-chlorobenzoyl)-semicarbazides. | Definition | ChEBI: An acyl chloride consisting of benzoyl chloride having a chloro substituent in the para-position. | General Description | 4-Chlorobenzoyl chloride is an acyl chloride. It reacts with 2-amino-2-seleno-5,5-dimethyl-1,3,2-dioxaphosphorinane to yield the respective N-acyl selenophosphoramides. |
| 4-Chlorobenzoyl chloride Preparation Products And Raw materials |
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