Cas 369-45-9,2-(4-fluorophenyl)-2-oxoethyl 4-nitrobenzoate

369-45-9

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Basic information

Product Name: 2-(4-fluorophenyl)-2-oxoethyl 4-nitrobenzoate
Synonyms: 2-(4-fluorophenyl)-2-oxoethyl 4-nitrobenzoate
CAS NO:369-45-9
Molecular Formula: C₁₅H₁₀FNO₅
Molecular Weight: 303.2420032
EINECS: N/A
Product Categories: N/A
Mol File: 369-45-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-(4-fluorophenyl)-2-oxoethyl 4-nitrobenzoate(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-fluorophenyl)-2-oxoethyl 4-nitrobenzoate(369-45-9)
EPA Substance Registry System: 2-(4-fluorophenyl)-2-oxoethyl 4-nitrobenzoate(369-45-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 369-45-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 369-45-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 369-45:
(5*3)+(4*6)+(3*9)+(2*4)+(1*5)=79
79 % 10 = 9
So 369-45-9 is a valid CAS Registry Number.

369-45-9Upstream product

369-45-9Downstream Products

369-45-9Relevant academic research and scientific papers

ONE STEP PROCESS FOR REGIOSELECTIVE SYNTHESIS OF α-ACYLOXY CARBONYLS

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Page/Page column 8; 9; 10, (2015/01/06)

A regioselective N-Heterocyclic Carbene (NHC) catalyzed one step process for high yield synthesis of α-acyloxy carbonyl compounds is disclosed.

N-Heterocyclic carbene catalyzed regioselective oxo-acyloxylation of alkenes with aromatic aldehydes: A high yield synthesis of α-acyloxy ketones and esters

Reddi, Rambabu N.,Malekar, Pushpa V.,Sudalai, Arumugam

supporting information, p. 6477 - 6482 (2013/09/24)

An N-heterocyclic carbene (NHC)-catalyzed reaction of alkenes with aromatic aldehydes providing for a high yield synthesis of α-acyloxy ketones and esters has been described. This unprecedented regioselective oxidative process employs NBS and Et3N in stoichiometric amounts and O2 (1 atm) as an oxidant under ambient conditions in DMSO as a solvent.

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