Detail of > 1668-54-8
- CAS Number:
- 1668-54-8
- Name:
1,3,5-Triazin-2-amine,4-methoxy-6-methyl-
- Superlist Name:
- 2-Amino-4-methoxy-6-methyl-1,3,5-triazine
- Formula:
- C5H8N4O
- Molecular Structure:

- Synonyms:
- 2-Amino-4-methoxy-6-methyl-1,3,5-triazine;2-Amino-4-methoxy-6-methyl-s-triazine;2-Amino-4-methyl-6-methoxy-s-triazine;4-Methoxy-6-methyl-1,3,5-triazin-2-amine;A 4098;CV 399;IN-A 4098;s-Triazine,2-amino-4-methoxy-6-methyl- (7CI,8CI);
- Molecular Weight:
- 140.17
- EINECS:
- 216-790-7
- Density:
- 1.255 g/cm3
- Melting Point:
- 258-261 °C(lit.)
- Boiling Point:
- 346.4 °C at 760 mmHg
- Flash Point:
- 163.3 °C
- Appearance:
- off-white to light yellow powder
- Hazard Symbols:
Xn- Risk Codes:
- 22-36/37/38
- Safety:
- 26-36-37/39Details
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- 1668-54-81,3,5-Triazin-2-amine,4-methoxy-6-methyl-
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Reference
- Photochemical behavior of chlorsulfuron in water and in adsorbed phase
- Photochemical behavior of chlorsulfuron in water and in adsorbed phase. Herrmann, M.; Kotzias, D.; Korte, F. (Inst. Oekol. Chem., Ges. Strahlen- Umweltforsch. m.b.H. Muenchen, Freising-Attaching D-8050, Fed. Rep. Ger.). Chemosphere, 14(1), 3-8 (English) 1985. CODEN: CMSHAF. ISSN: 0045-6535. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemical Bioregulators) The photochem. of the herbicide chlorsulfuron [64902-72-3] was investigated in MeOH [67-56-1], distd. water, natural creek-water, on silica gel and on montmorillonite [1318-93-0] surfaces. The rate of degrdn. was detd. in outdoor and indoor expts. simulating tropospheric conditions (l > 290 nm). Two major photoproducts, i.e., 2-chlorobenzene sulfonamide [6961-82-6] and 2-methoxy-4-methyl-6-amino-1,3,5-triazine [1668-54-8], were identified in all cases.
- Herbicidal and plant growth regulating sulfonyl urea and sulfonyl carbamates as intermediates
- Herbicidal and plant growth regulating sulfonyl urea and sulfonyl carbamates as intermediates. Meyer, Willy; Foery, Werner; Toepfl, Werner (Ciba-Geigy A.-G. , Switz.). Eur. Pat. Appl. EP 101407 A2 22 Feb 1984, 18 pp. DESIGNATED STATES: R: CH, DE, FR, GB, LI. (German). (European Patent Organization). CODEN: EPXXDW. CLASS: IC: C07D405-12; C07D409-12; C07D403-12; C07D401-12; C07D239-42; C07D239-52; C07D239-46; C07D239-48; C07D251-16; C07D251-44; C07D251-26. ICA: C07D333-38; C07C143-83; C07C155-02. APPLICATION: EP 83-810318 13 Jul 1983. PRIORITY: CH 82-4396 19 Jul 1982. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 5 Fungicidal and plant growth regulating (no data) I [R = (un)substituted Ph, furyl, thienyl, pyrrolyl, pyridinyl; R1 = alkyl, alkoxy, haloalkoxy; R2 = alkylthio, halo, amino, R1; X = N, CH] were prepd. Thus, H2NCO2Et was acylated with 2-(F2CHO)C6H4SO2Cl to give 23.3% 2-(F2CHO)C6H4SO2NHCO2Et. This was treated with 2-amino-4-methoxy-6-methyl-1,3,5-triazine to give 23.In this experiment, several chemicals are used like 1668-54-8 and 67359-63-1 1% I [R = 2-(F2CHO)C6H4, R1 = MeO, R2 = Me, X = N]. Fifteen other carbamate intermediates were prepd. .
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