1,3-Dichloropropene is a xenobiotic compound that requires catabolic enzymes for breakdown. The compound's evolutionary history suggests a possible precursor enzyme with dehalogenase or decarboxylase activity. AI generated definition based on: Bioorganic Chemistry, 2004 ...
Hydrolysis is the major pathway for fumigant 1,3‐dichloropropene (1,3‐D) degradation in water and soil, yet the process is not well understood. Experiments were conducted to investigate the effect of various environmental factors on the rate of 1,3‐D hydrolysis. Cis‐, trans‐1,3‐D ...
CIS-1,3-DICHLOROPROPENE CAS:10061-01-5 MW:110.965 MF:C3H4Cl2 CIS-1,3-DICHLOROPROPENE, with the chemical formula C3H4Cl2 and CAS registry number 10061-01-5, is a compound known for its applications in agriculture and industry. This colorless liquid, also referred to as cis-1,3-dichloropro...
1,3-dichloropropene Exists in two forms, cis-1,3-dichloropropene, CAS number 10061-01-5, trans-1,3-dichlorpropene, CAS number 10061-02-6, or as the isomeric mixture. Used as a soil fumigant (nematocide). Animal carcinogen and suspected human carcinogen. Reference: ATSDR document, Se...
Subsurface concentrations of the biologically active compounds cis- and trans-1,3-dichloropropene (1,3-D) and chloropicrin (CP) were determined in soil at two adjacent injection traces and midpoint between the two traces in plastic-covered field beds after injection of the fumigant Telone C35 ...
1,2-Benzenediol, 3,4,5,6-tetrachloro- 1,2-Benzenediol, 4,4'-(1,1-dioxido-3H-2,1-benzoxathiol-3-ylidene) bis- 1,2-Benzenediol, 4,4'-(3H-2,1-benzoxathiol-3-ylidene) bis-, S,S-dioxide (9CI) 1,2-Benzenediol, 4,5-dichloro- ...
E/Z-1,3-Dichloropropene D 75-29-6 isopropyl chloride E 590-21-6 propenyl chloride F 107-05-1 3-chloroprop-1-ene Conditions ConditionsYield With aluminum oxide; copper dichloride; dibenzoyl peroxide at 489.9℃; for 0.000555556h; Product distribution; Mechanism; also other temperatur...
We have developed a fluorination protocol by adapting readily available and sufficiently stable CpFluors as a novel class of deoxyfluorination reagents that contain an all-carbon scaffold. We found that the electronic nature of the aryl substituents on thegem-difluorocyclopropene scaffold is critical ...
Information also provided for 3,600 nuclides and 4,400 nuclide decay modes.Editor's note: Some chemicals in this database contain more information than others due to the original reason this information was collected and how the compilation was accomplished....
Among such monomers, functional 1,3-butadiene derivatives are selected as the next target monomers, since 1,3-butadiene monomers are similar in anionic reactivity to styrene monomers and the living chain-end anions have reactivities roughly comparable to that of living polystyrene.1,2 Accord...