| Identification | Back Directory | [Name]
PROSULFOCARB | [CAS]
52888-80-9 | [Synonyms]
DEFI
BOXER
arkade
r15574
PROSULFOCARB
prosulfocarb (bsi,iso)
boxer(iciagrochemicals)
benzyldipropylthiolcarbamate
S-BENZYL DIPROPYLTHIOCARBAMATE
s-benzyldipropylthiolcarbamate
S-BENZYL N,N-DIPROPYLTHIOCARBAMATE)
dipropylthio-carbamicacis-benzylester
s-(phenylmethyl)dipropylcarbamothioate
PROSULFOCARB PESTANAL (S-BENZYLDI-PROPY
dipropyl-carbamothioicacis-(phenylmethyl)ester
S-benzyl N,N-dipropylthiocarbamate prosulfocarb
Carbamothioic acid, dipropyl-, S-(phenylmethyl) ester | [EINECS(EC#)]
401-730-6 | [Molecular Formula]
C14H21NOS | [MDL Number]
MFCD00145179 | [MOL File]
52888-80-9.mol | [Molecular Weight]
251.39 |
| Hazard Information | Back Directory | [Air & Water Reactions]
Thio and dithiocarbamates slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids. | [Reactivity Profile]
PROSULFOCARB is a thiocarbamate. Flammable gases are generated by the combination of thiocarbamates and dithiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates and dithiocarbamates are incompatible with acids, peroxides, and acid halides. | [Uses]
Prosulfocarb is a pesticide used in the protection of crops such as barley for its herbicidal activity. | [Definition]
ChEBI: A monothiocarbamic ester that is carbamothioic S-acid substituted by two propyl groups at the nitrogen atom and a benzyl group at the the sulfur atom. | [Synthesis Reference(s)]
Tetrahedron, 49, p. 2403, 1993 DOI: 10.1016/S0040-4020(01)86319-5 |
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