Weight | 88.11 g/mol |
---|---|
Formula | C3H8N2O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
1,3-DIMETHYLUREA (96-31-1)
Score:
#1122 in Biochemistry
,
#2861 in Biology
,
#3582 in Chemistry
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- KINETIC ANALYSIS OF THE FLUORESCENCE INDUCTION IN 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA POISONED CHLOROPLASTS (Photochemistry and Photobiology, 1975)
- The action of some derivatives of phenylurethan and of 3-phenyl-1, 1-dimethylurea on the Hill reaction. (Biochimica et Biophysica Acta, 1956)
- The number of sites sensitive to 3-(3,4-dichlorophenyl)-1,1-dimethylurea,3-(4-chlorophenyl)-1,1-dimethylurea and 2-chloro-4-(2-propylamino)-6-ethylamino-s-triazine in isolated chloroplasts. (Biochimica et Biophysica Acta, 1965)
- Hydrogen bonding and polyurethane morphology. II. Spectroscopic, thermal and crystallization behavior of polyether blends with 1,3-dimethylurea and a model urethane compound (Polymer, 2002)
- The Pesticide 3-(3,4-Dichlorophenyl)-1,1-dimethylurea (Diuron) Immobilized on Silica Gel Surface (Journal of Colloid and Interface Science, 2001)
- Mode of action of 3-(3,4-dichlorophenyl)-1,1-dimethylurea. Evidence that the inhibitor competes with plastoquinone for binding to a common site on the acceptor side of Photosystem II (Biochimica et Biophysica Acta, 1982)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 -
SMILESCNC(=O)NC
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InChIKeyMGJKQDOBUOMPEZ-UHFFFAOYSA-N
- Pubchem - 1,3-DIMETHYLUREA
- Wikipedia - 1,3-dimethylurea
Dimethylurea (DMU) (IUPAC systematic name: 1,3-Dimethylurea ) is a urea derivative and used as an intermediate in organic synthesis. It is a colorless crystalline powder with little toxicity.
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Synthesis
Methylboronic acid
+
Reactant
(Chan-Lam coupling reaction)
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