CAS 3553-80-8
:Carbamic acid, N,N-diethyl-, ethyl ester
Description:
Carbamic acid, N,N-diethyl-, ethyl ester, with the CAS number 3553-80-8, is an organic compound that belongs to the class of carbamates. It is characterized by the presence of a carbamic acid functional group, which is linked to two ethyl groups and an ethyl ester moiety. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents and exhibits moderate stability under standard conditions. The compound is primarily used in agricultural applications, particularly as a pesticide or herbicide, due to its ability to inhibit certain enzymes in pests. Its chemical structure allows for interactions with biological systems, which can lead to both desired effects in pest control and potential toxicity to non-target organisms. Safety data sheets indicate that it should be handled with care, as it may pose health risks upon exposure. Proper storage and handling procedures are essential to mitigate any hazards associated with its use.
Formula:C7H15NO2
InChI:InChI=1S/C7H15NO2/c1-4-8(5-2)7(9)10-6-3/h4-6H2,1-3H3
InChI key:InChIKey=VAJCYQHLYBTSHG-UHFFFAOYSA-N
SMILES:N(C(OCC)=O)(CC)CC
Synonyms:- BRN 1755148
- Diethylcarbamic acid ethyl ester
- 4-04-00-00377 (Beilstein Handbook Reference)
- Carbamic acid, diethyl-, ethyl ester
- Ethyl N,N-diethylcarbamate
- Ethyl diethylcarbamate
- Diethylcarbamic acid, ethyl ester
- NSC 24699
- Ethyl N,N-diethyl carbamate
- Carbamic acid, N,N-diethyl-, ethyl ester
- AI3-16945
- Diethyl urethane
- Ethyl N,N-diethylcarbamate
- See more synonyms
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Found 4 products.
Ethyl N,N-diethylcarbamate
CAS:<p>Ethyl N,N-diethylcarbamate is a potent inducer of the CYP3A4 enzyme and has been shown to cause cell lysis. It is a cyclic peptide that belongs to the antimicrobial peptides group. Ethyl N,N-diethylcarbamate has been shown to bind to bacterial dna and human liver cells as well as human erythrocytes. This drug also induces DNA strand breaks in both wild-type and mutant strains of Escherichia coli. Ethyl N,N-diethylcarbamate also causes an increase in nitrite levels in mouse models. The chemical structure of this compound is C6H11NO2 with a molecular weight of 149.18 g/mol. It has three diastereomers: R-(+), S-(+), and R-(−).</p>Formula:C7H15NO2Purity:Min. 95%Molecular weight:145.2 g/mol




