4-Chlorobenzoyl chloride

4-Chlorobenzoyl chloride
  • CAS No.:122-01-0

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
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4-Chlorobenzoyl chloride Basic information
Uses
Product Name:4-Chlorobenzoyl chloride
Synonyms:LABOTEST-BB LTBB000569;4-Chlorobenzoyl chloride, 99+% 5ML;4-CHLOROBENZOYL CHLORIDE FOR SYNTHESIS;Chlorobenzene forMyl chloride;4-chloro-benzoylchlorid;Benzoyl chloride, 4-chloro-;Benzoyl chloride, p-chloro-;Benzoylchloride,4-chloro-
CAS:122-01-0
MF:C7H4Cl2O
MW:175.01
EINECS:204-515-3
Product Categories:ACIDHALIDE;Absolute Configuration Determination (Exciton Chirality CD Method);Analytical Chemistry;Enantiomer Excess & Absolute Configuration Determination;Exciton Chirality CD Method (for Hydroxyl Groups);Acid Halides;Carbonyl Compounds;Organic Building Blocks;Absolute Configuration Determination
Mol File:122-01-0.mol
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.
form Liquid
color Clear colorless to faintly colored
explosive limit1.5-15%(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.
LogP2.52 at 25℃
CAS DataBase Reference122-01-0(CAS DataBase Reference)
NIST Chemistry Reference4-Chlorobenzoic acid chloride(122-01-0)
EPA Substance Registry SystemBenzoyl chloride, 4-chloro- (122-01-0)
Safety Information
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
MSDS Information
ProviderLanguage
4-Chlorobenzoyl chloride English
SigmaAldrich English
ACROS English
ALFA English
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 Propertiesliquid
Uses4-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.
Uses4-Chlorobenzoyl chloride was used to synthesize 4-chlorobenzoyl CoA by reacting it with CoA in KHCO3 buffer.
DefinitionChEBI: An acyl chloride consisting of benzoyl chloride having a chloro substituent in the para-position.
General Description4-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.

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