CAS 111479-05-1: PROPAQUIZAFOP
Formula:C22H22ClN3O5
InChI:InChI=1S/C22H22ClN3O5/c1-14(2)26-29-11-10-28-22(27)15(3)30-17-5-7-18(8-6-17)31-21-13-24-20-12-16(23)4-9-19(20)25-21/h4-9,12-13,15H,10-11H2,1-3H3/t15-/m1/s1
InChI key:InChIKey=FROBCXTULYFHEJ-OAHLLOKOSA-N
SMILES:O(C1=NC2=C(N=C1)C=C(Cl)C=C2)C3=CC=C(O[C@@H](C(OCCON=C(C)C)=O)C)C=C3
Synonyms:- (R)-2(((1-methylethylidene)amino)oxy)ethyl-2-(4-((6-chloro-2-quinoxalinyl)oxy)phenoxy)propanoate
- (R)-2-(Propan-2-ylideneaminooxy)ethyl 2-(4-(6-chloroquinoxalin-2-yloxy)phenoxy)propanoate
- (R)-Lidene)Amino)Oxy)Ethyleste
- 2-(4-((6-Chloro-2-Quinoxalinyl)Oxy)Phenoxy)-Propanoicaci2-(((1-Methylethy
- 2-Isopropylideneamino-Oxyethyl(R)-2-(4-(6-Chloroquinoxalin-2-Yloxy)Phenoxy)P
- 2-[(Propan-2-Ylideneamino)Oxy]Ethyl 2-{4-[(6-Chloroquinoxalin-2-Yl)Oxy]Phenoxy}Propanoate
- Agil
- Correct
- Propanoic acid, 2-[4-[(6-chloro-2-quinoxalinyl)oxy]phenoxy]-, 2-[[(1-methylethylidene)amino]oxy]ethyl ester, (2R)-
- Propanoic acid, 2-[4-[(6-chloro-2-quinoxalinyl)oxy]phenoxy]-, 2-[[(1-methylethylidene)amino]oxy]ethyl ester, (R)-
- Ro 17-3664
- See more synonyms
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Found 8 products.
GB 23200.121-2021 Pesticide Mixture 8 50 µg/mL in Acetonitrile:Methanol
CAS:Controlled Product- 101205-02-1
- 107534-96-3
- 111479-05-1
- 111988-49-9
- 117428-22-5
- 119446-68-3
- 121-21-1
- 129630-19-9
- 131860-33-8
- 133855-98-8
- 134098-61-6
- 135186-78-6
- 143390-89-0
- 148477-71-8
- 153233-91-1
- 153719-23-4
- 19666-30-9
- 2312-35-8
- 238410-11-2
- 283594-90-1
- 28434-01-7
- 39300-45-3
- 39515-41-8
- 40596-69-8
- 50512-35-1
- 51-03-6
- 51338-27-3
- 51630-58-1
- 52645-53-1
- 52918-63-5
- 55179-31-2
- 55219-65-3
- 69806-50-4
- 70288-86-7
- 76578-14-8
- 77501-63-4
- 77501-90-7
- 80844-07-1
- 82657-04-3
- 83657-24-3
- 83-79-4
- 850881-70-8
- 88671-89-0
- 935545-74-7
- 94361-06-5
- 95737-68-1
Color and Shape:MixturePropaquizafop
CAS:Propaquizafop, a phenoxyisopropionic acid derivative, is used as a herbicide.Formula:C22H22ClN3O5Purity:98%Color and Shape:Colourless-To-Brown CrystalsMolecular weight:443.88LC PestiMix 2 10 µg/mL in Acetonitrile
CAS:- 101-42-8
- 103361-09-7
- 105512-06-9
- 111479-05-1
- 111988-49-9
- 113507-06-5
- 114311-32-9
- 116714-46-6
- 120116-88-3
- 122-34-9
- 13360-45-7
- 134098-61-6
- 134605-64-4
- 135158-54-2
- 139-40-2
- 144550-36-7
- 145701-23-1
- 14816-18-3
- 149979-41-9
- 156052-68-5
- 158062-67-0
- 16118-49-3
- 161326-34-7
- 1634-78-2
- 1646-87-3
- 165252-70-0
- 16655-82-6
- 168316-95-8
- 1746-81-2
- 177406-68-7
- 181587-01-9
- 18691-97-9
- 1912-26-1
- 1967-16-4
- 1982-47-4
- 19937-59-8
- 208465-21-8
- 2163-69-1
- 2164-08-1
- 22248-79-9
- 23947-60-6
- 24151-93-7
- 24307-26-4
- 24691-76-7
- 2631-40-5
- 2655-14-3
- 27218-04-8
- 272451-65-7
- 283594-90-1
- 29104-30-1
- 298-01-1
- 298-02-2
- 3060-89-7
- 30614-22-3
- 330-54-1
- 33693-04-8
- 34622-58-7
- 34681-10-2
- 34681-23-7
- 361377-29-9
- 374726-62-2
- 3761-42-0
- 3766-60-7
- 3766-81-2
- 37764-25-3
- 3878-19-1
- 39196-18-4
- 4147-51-7
- 500008-45-7
- 5234-68-4
- 53380-22-6
- 55814-41-0
- 57646-30-7
- 58810-48-3
- 62610-77-9
- 64628-44-0
- 64902-72-3
- 66063-05-6
- 66215-27-8
- 66840-71-9
- 68157-60-8
- 71283-80-2
- 71422-67-8
- 72490-01-8
- 73250-68-7
- 74223-64-6
- 76578-14-8
- 79241-46-6
- 79277-27-3
- 81405-85-8
- 81412-43-3
- 82097-50-5
- 82558-50-7
- 83055-99-6
- 83-79-4
- 865318-97-4
- 935545-74-7
- 93-71-0
- 94125-34-5
- 94593-91-6
- 950-10-7
- 999-81-5
Color and Shape:MixturePropaquizafop
CAS:Controlled ProductApplications Propaquizafop is used in the studies of the pesticides residue in tomatoes and cucumbers and the associated health risks. References Lozowicka, B., et al.: Environ. Monit. Assess., 187, 1 (2015)Formula:C22H22ClN3O5Color and Shape:WhiteMolecular weight:443.88(R)-2-(Propan-2-ylideneaMinooxy)ethyl 2-(4-(6-chloroquinoxalin-2
CAS:(R)-2-(Propan-2-ylideneaminooxy)ethyl 2-(4-(6-chloroquinoxalin-2-yl)phenoxy)acetate (CQA) is an inhibitor of bacterial disease activity. CQA has been shown to inhibit the growth of a number of bacterial strains, including Escherichia coli, Salmonella enterica serovar Typhimurium, and Mycobacterium smegmatis. The terminal residues of CQA have been identified as 4-hydroxybenzoic acid and 2-[(1S,2S)-2-methylcyclohexyl]propane-1,3 diol. The enzyme inhibition mechanism for this drug is not fully understood but may be due to its ability to bind to the active site of enzymes that catalyze reactions involving metal chelates or hydrolysis of solanum tuberosum. CQA also binds to mitochondrialFormula:C22H22ClN3O5Purity:Min. 95%Molecular weight:443.88 g/mol
