20184-94-5 Usage
Chelating agent
Used in analytical chemistry This compound forms stable complexes with metal ions, making it useful for various applications in the field of chemistry and biochemistry.
Methyl ester derivative
Of 1-methylhydrazine-1-dithiocarboxylic acid 1-Methylhydrazine-1-dithiocarboxylic acid methyl ester is derived from 1-methylhydrazine-1-dithiocarboxylic acid by the addition of a methyl ester group.
Yellowish liquid
With a pungent odor The compound has a yellowish appearance and a strong, unpleasant smell.
Research and industrial applications
Primarily used in research laboratories and industrial settings 1-Methylhydrazine-1-dithiocarboxylic acid methyl ester is mainly utilized in these environments due to its chelating properties.
Potential health hazards
Proper safety precautions required Handling this chemical may pose health risks, so it is essential to follow appropriate safety measures when working with it.
Check Digit Verification of cas no
The CAS Registry Mumber 20184-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,8 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20184-94:
(7*2)+(6*0)+(5*1)+(4*8)+(3*4)+(2*9)+(1*4)=85
85 % 10 = 5
So 20184-94-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H8N2S2/c1-5(4)3(6)7-2/h4H2,1-2H3
20184-94-5Relevant articles and documents
On Triazoles. XXVIII. Synthesis of Isomeric 1,2,4-Triazolylcarbothiohydrazides
Barkoczy, Jozsef,Reiter, Jozsef
, p. 1677 - 1683 (2007/10/02)
Different 3a, 3b, 9, 10 and 12 type 5-amino-1,2,4-triazolylcarbothiohydrazide isomers representing all possible isomeric types derived from 5-amino-1,2,4-triazoles were synthesised from the corresponding 5-amino-1,2,4-triazolyldithiocarbonates and hydrazines.HPLC measurements proved that in case of monosubstituted hydrazines the steric press in the intermediate 6 caused besides formation of the expected derivative 3a the formation of compounds 4 and 5, too, while the intermediate 7 yielded only 3b.Thermal rearangement of derivatives 3a in acetic acid led to isomers 9 and 10, respectively.
