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    CLORANSULAM-METHYL

    CLORANSULAM-METHYL ??? ???
    ?? ??:
    147150-35-4
    ???:
    CLORANSULAM-METHYL
    ???(??):
    xde-565;CLORANSULAM-METHYL;ChloransulaM-Methyl;cloransulam-methyl (bsi, pa iso, ansi);Cloransulam methyl@100 μg/mL in Acetonitrile;Cloransulam-methyl Solution in Acetonitrile/Methanol, 1000μg/mL;Methyl 3-chloro-N-(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidin-2-ylsulfonyl)anthranilate;Methyl 3-chloro-2-[(5-ethoxy-7-fluoro-[1,2,4]triazolo[5,1-c]pyrimidin-2-yl)sulfonylamino]benzoate;Methyl 3-chloro-2-{[(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidine-2-yl)sulfonyl]amino}benzoate;3-Chloro-2-[[(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidin-2-yl)sulfonyl]amino]benzoic acid, Methyl ester
    CBNumber:
    CB0691826
    ???:
    C15H13ClFN5O5S
    ??? ??:
    429.81
    MOL ??:
    147150-35-4.mol

    CLORANSULAM-METHYL ??

    ???
    216-218 °C
    ??
    1.538 g/cm3
    ?? ??
    0-6°C
    ??? ??
    neat
    ?? ?? (pKa)
    3.97±0.50(Predicted)
    BRN
    7501727
    CAS ??????
    147150-35-4
    EPA
    Cloransulam-methyl (147150-35-4)
    ??
    • ?? ? ?? ??
    • ?? ? ???? ?? (GHS)
    ??? ?? Xn,N
    ?? ???? ?? 20-50
    ????? 61
    ????(UN No.) UN 3077 9 / PGIII
    WGK ?? 3
    ?? ?? ??? 147150-35-4(Hazardous Substances Data)
    ????(GHS):
    ?? ?: Warning
    ??·?? ??:
    ?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
    H332 ???? ??? ?? ?? ?? ?? ?? 4 ?? P261, P271, P304+P340, P312
    H410 ??? ??? ?? ????? ?? ??? ?? ????? ?? - ?? ?? 1 ?? P273, P391, P501
    ??????:
    P273 ???? ???? ???.
    P501 ...? ??? / ??? ?? ???.

    CLORANSULAM-METHYL C??? ??, ??, ??

    ??

    ChEBI: The methyl ester of cloransulam. An inhibitor of acetohydroxyacid synthase (AHAS), it prevents the synthesis of amino acids in plants and is used as a herbicide for the control of post-emergence control of broad-leaved weeds in soybeans. It is not approved for use within the European Area.

    ?? ?? ??

    When 14C-cloransulam methyl is incubated with soils, the degradation proceeds via the hydrolysis of the ester group and O-de-ethylation on the triazolopyrimidine ring to yield the three identified metabolites, cloransulam, 5-hydroxycloransulam methyl, and 5-hydroxycloransulam. These metabolites are significantly less phytotoxic than the parent herbicide.

    CLORANSULAM-METHYL ?? ?? ? ???

    ???

    ?? ??


    CLORANSULAM-METHYL ?? ??

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