619-33-0 Usage
Uses
Used in Pharmaceutical Industry:
2,2-Dichloro-1,1-diethoxyethane is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique chemical properties make it a valuable component in the creation of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2-Dichloro-1,1-diethoxyethane serves as a key intermediate in the synthesis of pesticides and other agricultural chemicals. Its involvement in the production process helps to ensure the effectiveness and quality of these products, supporting agricultural productivity and crop protection.
Used in Specialty Chemicals Production:
2,2-Dichloro-1,1-diethoxyethane is utilized as an intermediate in the manufacture of specialty chemicals, which are often used in specific applications due to their unique properties. Its versatility in chemical reactions allows for the development of tailored chemical products for various industries.
Used as a Solvent:
2,2-Dichloro-1,1-diethoxyethane's solvent properties make it suitable for use in various industrial applications where a solvent with specific characteristics is required. Its ability to dissolve a wide range of substances without causing unwanted reactions is particularly beneficial in processes that demand precision and control.
Check Digit Verification of cas no
The CAS Registry Mumber 619-33-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 619-33:
(5*6)+(4*1)+(3*9)+(2*3)+(1*3)=70
70 % 10 = 0
So 619-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H12Cl2O2/c1-3-9-6(5(7)8)10-4-2/h5-6H,3-4H2,1-2H3
619-33-0Relevant articles and documents
Reactions of α-monochloro- and α,α-dichloro-β-oxoaldehyde acetals with bases
Guseinov
, p. 663 - 665 (2007/10/03)
α,α-Dichloro-β-oxoaldehyde diethyl acetals decompose under the action of bases (NaOH, MeONa) with cleavage of the carbon-carbon bond and formation of carboxylic acids or their esters and the dichloroacetaldehyde diethyl acetal carbanion. The latter reacts in situ with benzaldehyde to form stable α-chloro-α,β-epoxyacetal. α-Chloro-α-formyl-γ-butyrolactone diethyl acetal is transformed into α-chloro-α-diethoxymethyl-γ-hydroxybutyric acid under the action of an alkali.
Products and reaction pats in the liquid phase oxidation of trans-1,2-dichloroethene with oxygen
Griesbaum, Karl,Hayes, Michael P.,Werli, Vera
, p. 1366 - 1370 (2007/10/02)
Ultraviolet initiated liquid phase oxidation of neat trans-1,2-dichloroethene (1a) with oxigen at 30 deg C afforded ca. 45percent of the combined Cl-products CO, CO2, and phosgene as well as nine oxygenated and nine non-oxygenated chlorinated organic products.Major oxigenated products were cis- and trans-2,3-dichlorooxirane (6a, b) and 1,2,2-trichloroethyl formate (13); minor products were e.g., meso and rac bis(1,2,2-trichloroethyl)ether (11c, d) and dichloromethyl 1,2,2,-trichloroethyl ether (12).The mode of formation of all products is rationalized by a unified reaction scheme.
