13398-04-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This is the common name used to refer to the compound in the field of chemistry.
Explanation
The compound is in a liquid state at room temperature and is colorless in appearance.
Explanation
These are the primary applications of the compound in different industries.
Explanation
The compound can easily catch fire and burn, posing a risk in certain conditions.
Explanation
Contact with the compound can cause discomfort and harm to the skin, eyes, and respiratory system.
Explanation
If released into the environment, the compound can have negative effects on aquatic life, potentially disrupting ecosystems.
Explanation
Due to its flammable nature and potential health hazards, it is crucial to follow safety protocols when handling this chemical compound.
Physical State
Colorless liquid
Uses
a. Intermediate in the production of pharmaceuticals, perfumes, and flavorings
b. Solvent in various chemical processes
c. Reagent in organic synthesis
Flammability
Flammable
Health Hazards
a. Skin irritation
b. Eye irritation
c. Respiratory system irritation
Environmental Impact
Harmful to aquatic organisms
Safety Precautions
Handle with care
Check Digit Verification of cas no
The CAS Registry Mumber 13398-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,9 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13398-04:
(7*1)+(6*3)+(5*3)+(4*9)+(3*8)+(2*0)+(1*4)=104
104 % 10 = 4
So 13398-04-4 is a valid CAS Registry Number.
13398-04-4Relevant articles and documents
Chlorination of Carboxylic Acid Derivatives. IX. Liquid Phase Chlorination of Aliphatic C2-C8 Alkyl Acetates. EI Mass Spectra of Monochlorinated Esters
Korhonen, Ilpo O. O.
, p. 39 - 46 (2007/10/02)
A series of aliphatic alkyl acetates from ethyl to octyl acetate was chlorinated in the liquid phase in order to obtain monochlorinated products.The chlorination of esters was carried out with chlorine in the liquid phase in the absence and in the presence of benzene and with sulfuryl chloride in the presence of Bz2O2.The products were determined by gas-liquid chromatography and gas-liquid chromatography-mass spectrometry.Chlorination is appreciably deactivated at the 1-position, particularly with SO2Cl2, the deactivation at the 2-position being strongest with Cl2 in the presence of benzene.The amounts of 1-chloro and ω-chloro isomers constituted the greatest disparity between the chlorination methods.The most characteristic mass spectral fragment ions of the 35 chlorinated alkyl acetates are given.
