6287-87-2 Usage
Description
Ethyl (phenylcarbonyl)dithiocarbamate is a chemical compound with the molecular formula C10H13NO2S2. It is a versatile substance known for its fungicidal properties and its use in the rubber manufacturing industry.
Uses
Used in Agriculture:
Ethyl (phenylcarbonyl)dithiocarbamate is used as a fungicide for protecting crops and plants from a wide range of plant pathogenic fungi. It functions by inhibiting the growth and reproduction of these fungi, thereby ensuring the health and productivity of agricultural produce.
Used in Rubber Manufacturing:
In the rubber industry, ethyl (phenylcarbonyl)dithiocarbamate is utilized in the manufacturing process. Its application contributes to the production of rubber goods with desired properties, such as elasticity and durability.
Safety Considerations:
Ethyl (phenylcarbonyl)dithiocarbamate is known to have moderate toxicity to humans. It can potentially cause adverse effects on the skin, eyes, and respiratory system. Therefore, it is crucial to follow proper handling procedures and adopt protective measures when working with this chemical to minimize health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 6287-87-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6287-87:
(6*6)+(5*2)+(4*8)+(3*7)+(2*8)+(1*7)=122
122 % 10 = 2
So 6287-87-2 is a valid CAS Registry Number.
6287-87-2Relevant articles and documents
S-ethyl N-benzoyldithiocarbamate: Two independent hydrogen-bonded R 22(8) dimers of different symmetry linked into chains by a C-H...π(arene) interaction
Low, John N.,Cobo, Justo,Insuasty, Henry,Estrada, Martin,Cortes, Edward,Glidewell, Christopher
, p. o483-o485 (2004)
The title compound, C10H11NOS2, crystallizes with Z′ = 2 in space group C2/c. The molecules are linked by two N-H...S hydrogen bonds [H...S = 2.60 and 2.62 A, N...S = 3.350 (2) and 3.490 (2) A, and N-H...S = 143 and 172°] into two distinct types of R22(8) dimer, viz. one generated by inversion and the other by a twofold rotation axis. A single C-H...π(arene) hydrogen bond links the two types of dimer into chains.
