58249-87-9

Basic information

• Product Name: 2-(BENZOYLOXYMETHYL)BENZOYL CHLORIDE
• Synonyms: 2-(BENZOYLOXYMETHYL)BENZOYL CHLORIDE;2-(HYDROXYMETHYL)BENZOYL CHLORIDE BENZOATE;2-(BENZOYLOXYMETHYL)BENZOYL CHLORIDE, ST AB.;2-(Benzoyloxymethyl)benzoic acid chloride;Einecs 261-186-9
• CAS NO: 58249-87-9
• Molecular Formula: C₁₅H₁₁ClO₃
• Molecular Weight: 274.7
• EINECS: 261-186-9
• Mol File: 58249-87-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 59-61 °C
• Boiling Point: 407.9°C at 760 mmHg
• Flash Point: 165.6°C
• Appearance: /
• Density: 1.281g/cm³
• Vapor Pressure: 7.28E-07mmHg at 25°C
• Refractive Index: 1.593
• Storage Temp.: 2-8°C
• BRN: 2131346
• CAS DataBase Reference: 2-(BENZOYLOXYMETHYL)BENZOYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(BENZOYLOXYMETHYL)BENZOYL CHLORIDE(58249-87-9)
• EPA Substance Registry System: 2-(BENZOYLOXYMETHYL)BENZOYL CHLORIDE(58249-87-9)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: UN 3261 8/PG 3
• WGK Germany: 3
• F: 10-21
• Hazardous Substances Data: 58249-87-9(Hazardous Substances Data)

Usage

General Description

2-(Benzoyloxymethyl)benzoyl chloride is a chemical compound with the molecular formula C15H11ClO3. It is a benzoyl chloride derivative, consisting of a benzoyloxy group attached to the carbon atom of a benzoyl group. 2-(BENZOYLOXYMETHYL)BENZOYL CHLORIDE is often utilized in organic synthesis as a reagent for the preparation of various organic compounds, including pharmaceuticals, pesticides, and dyes. It is a colorless to pale yellow liquid with a pungent odor and is highly reactive due to the presence of the benzoyl and benzoyloxymethyl groups. Additionally, it is important to handle this compound with caution as it is a corrosive substance that can cause skin and eye irritation, and respiratory issues if inhaled.

InChI:InChI=1/C15H11ClO3/c16-14(17)13-9-5-4-8-12(13)10-19-15(18)11-6-2-1-3-7-11/h1-9H,10H2

Upstream product

• 58249-83-5 2-(benzoyloxymethyl)benzoic acid 
• 98-88-4 benzoyl chloride 
• 87-41-2 2-benzofuran-1(3H)-one 

Downstream Products

• 1430334-89-6 C₁₈H₁₇NO₃ 
• 1430334-90-9 C₂₀H₂₁NO₃ 
• 1383575-36-7 2-(3-(methoxymethyl)-1,2,4-oxadiazol-5-yl)benzyl benzoate 
• 1383575-37-8 (2-(3-(methoxymethyl)-1,2,4-oxadiazol-5-yl)phenyl)methanol 
• 1383575-38-9 5-(2-(bromomethyl)phenyl)-3-(methoxymethyl)-1,2,4-oxadiazole 
• 1383575-39-0 2-(prop-2-yn-1-ylcarbamoyl)benzyl benzoate 
• 1243629-47-1 2-({[2-(3,4-dimethoxyphenyl)ethyl]amino}carbonyl)benzyl benzoate 
• 1010733-02-4 dimethyl 2-(benzoyloxymethyl)benzoylphosphonate 
• 395099-87-3 (2-{N-[3-(4-FLUOROPHENYL)-1H-INDAZOL-5-YL]CARBAMOYL}PHENYL)METHYL BENZOATE 
• 256498-96-1 3-[4-(2-benzoyloxymethylbenzoylamino)-5-ethylpyrimidin-2-yl]-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine 
• 635757-20-9 2-(((8-(1,3,3-trimethylbutoxy)quinolin-2-yl)amino)carbonyl)benzyl benzoate 
• 58249-89-1 2-methyl-N-(4-methylphenyl)-benzamide 
• 94411-34-4 2-<(3,4,5,6-Tetrahydro-3-oxo-2H-pyran-4-yl)carbonyl>benzylbenzoat 
• 94411-35-5 2-<4-<2-Hydroxy-2-(3,4,5,6-tetrahydro-3-oxo-2H-pyran-4-yliden)ethoxy>-1-oxobutyl>benzylbenzoat 

Relevant articles and documents

Aziridine ring-containing chiral ligands as highly efficient catalysts in asymmetric synthesis

Enantiomerically pure bidentate heteroorganic ligands built on an achiral skeleton containing hydroxyl and aziridine moieties as nucleophilic centers, capable of binding various organometallic reagents, have proven to be highly efficient catalysts in the enantioselective addition of diethylzinc and phenylethynylzinc to aryl and alkyl aldehydes to give the desired chiral products in high chemical yields (up to 90%) and with ees of up to 95%. The influence of the stereogenic center located in the carbon atom in the aziridine moiety on the stereochemical course of the reaction is reported.

SUBSTITUTED CYCLOHEXYL-1,4-DIAMINE DERIVATIVES WITH A CHAIN EXTENSION

The invention relates to substituted cyclohexyl-1,4-diamine derivatives, to a method for their production, to medicaments containing said compounds and to the use of substituted cyclohexyl-1,4-diamine derivatives for producing medicaments.

3,5-Diphenyl-1H-1,2,4-triazoles pharmaceutical compositions and uses

3,5-diphenyl-1H-1,2,4-triazoles with contragestational activity of the following formula STR1 wherein R may be located on one or the other of the two adjacent nitrogen atoms and may represent hydrogen or a group R5 CO-- wherein R5 is an aliphatic saturated or unsaturated hydrocarbyl containing from 1 to 20 carbon atoms, R1, R2 and R3, each independently are selected from hydrogen, lower alkyl and lower alkoxy or R2 and R3 together may represent a methylenedioxy group, and R4 is an aliphatic saturated or unsaturated hydrocarbyl group of from 1 to 20 carbons, with the proviso that when R is hydrogen or an R5 CO-- group wherein R5 contains 4 or less carbon atoms, R4 must contain 5 or more carbons. These compounds have proven to be highly effective in terminating pregnancy in several animal species after a single parenteral injection.