Product Name

  • Name

    methyldithiocarbazate

  • EINECS
  • CAS No. 5397-03-5
  • Article Data51
  • CAS DataBase
  • Density 1.314 g/cm3
  • Solubility
  • Melting Point 79 °C(Solv: benzene (71-43-2))
  • Formula C2H6N2S2
  • Boiling Point 207.3 °C at 760 mmHg
  • Molecular Weight 122.215
  • Flash Point 79.2 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 5397-03-5 (methyldithiocarbazate)
  • Hazard Symbols
  • Synonyms Carbazicacid, dithio-, methyl ester (7CI,8CI);Dithiocarbazic acid methyl ester;Hydrazine-S-methylcarbodithioate;Methyl dithiocarbazate;Methylhydrazinecarbodithioate;NSC 4423;S-Methyl dithiocarbazate;S-Methylhydrazinecarbodithioate;
  • PSA 95.44000
  • LogP 1.18880

Synthetic route

(S,S)-dimethyl trithiocarbonate
2314-48-9

(S,S)-dimethyl trithiocarbonate

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
With hydrazine hydrate In ethanol at 0℃; for 3h;91%
carbon disulfide
75-15-0

carbon disulfide

methyl iodide
74-88-4

methyl iodide

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
Stage #1: carbon disulfide With hydrazine hydrate; potassium hydroxide In water; isopropyl alcohol at 0 - 10℃; for 3h;
Stage #2: methyl iodide In water; isopropyl alcohol at 20℃; for 4h; Cooling with ice;
90%
Stage #1: carbon disulfide With hydrazine hydrate; potassium hydroxide In water; isopropyl alcohol at 0 - 10℃;
Stage #2: methyl iodide In water; isopropyl alcohol at 20℃;
86.5%
Stage #1: carbon disulfide With hydrazine hydrate; potassium hydroxide In water; isopropyl alcohol at 0 - 10℃; for 3h;
Stage #2: methyl iodide In water; isopropyl alcohol at 10℃; for 1h;
64.5%
carbon disulfide
75-15-0

carbon disulfide

hydrazine
302-01-2

hydrazine

methyl iodide
74-88-4

methyl iodide

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
With potassium hydroxide In water; isopropyl alcohol at 20℃; for 4h;90%
carbon disulfide
75-15-0

carbon disulfide

dimethyl sulfate
77-78-1

dimethyl sulfate

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
Stage #1: carbon disulfide With hydrazine hydrate; potassium hydroxide In water; isopropyl alcohol at 9 - 10℃;
Stage #2: dimethyl sulfate In water; isopropyl alcohol at 12 - 15℃;
78%
Stage #1: carbon disulfide With potassium hydroxide; hydrazine In isopropyl alcohol for 3.66667h;
Stage #2: dimethyl sulfate In isopropyl alcohol for 1h;
60.1%
Stage #1: carbon disulfide With hydrazine hydrate; potassium hydroxide In water; isopropyl alcohol at 10℃; for 3.66667h;
Stage #2: dimethyl sulfate In water; isopropyl alcohol at 15℃;
60.1%
S-ammonium hydrazinecarbodithiolate
5456-21-3

S-ammonium hydrazinecarbodithiolate

dimethyl sulfate
77-78-1

dimethyl sulfate

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In water
S-ammonium hydrazinecarbodithiolate
5456-21-3

S-ammonium hydrazinecarbodithiolate

methyl iodide
74-88-4

methyl iodide

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In water
methyl iodide
74-88-4

methyl iodide

ammonium salt of dithiocarbazic acid

ammonium salt of dithiocarbazic acid

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
With ethanol
methyl iodide
74-88-4

methyl iodide

dithiocarbazinate potassium

dithiocarbazinate potassium

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
carbon disulfide
75-15-0

carbon disulfide

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
With potassium hydroxide; hydrazine In isopropyl alcohol
dithiocarbonic acid hydrazide
471-32-9

dithiocarbonic acid hydrazide

methyl iodide
74-88-4

methyl iodide

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In water; isopropyl alcohol at 10℃; for 3.5h;18.5 g
In ethanol at 0℃; for 1.5h;
for 3.5h; Cooling with ice;
In water; isopropyl alcohol for 3h; Cooling with ice;
potassium hydrazine carbodithioate
26648-11-3

potassium hydrazine carbodithioate

methyl iodide
74-88-4

methyl iodide

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In ethanol
In ethanol at 0℃; for 5h;
With potassium hydroxide at 10℃;
carbon disulfide
75-15-0

carbon disulfide

hydrazine hydrate
7803-57-8

hydrazine hydrate

methyl iodide
74-88-4

methyl iodide

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
With potassium hydroxide at 0 - 5℃;
CH3N2S2(1-)*Na(1+)

CH3N2S2(1-)*Na(1+)

methyl iodide
74-88-4

methyl iodide

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In water; isopropyl alcohol for 1.5h; Cooling with ice;
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

malonic acid ethyl ester 5-oxo-pentyl ester

malonic acid ethyl ester 5-oxo-pentyl ester

malonic acid ethyl ester 5-(methylsulfanylthiocarbonyl-hydrazono)-pentyl ester

malonic acid ethyl ester 5-(methylsulfanylthiocarbonyl-hydrazono)-pentyl ester

Conditions
ConditionsYield
In ethanol for 10h; Heating;100%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

1-(3-((2-methoxyethoxy)methyl)pyridin-2-yl)ethan-1-one

1-(3-((2-methoxyethoxy)methyl)pyridin-2-yl)ethan-1-one

methyl (E)-2-(1-(3-((2-methoxyethoxy)methyl)pyridin-2-yl)ethylidene)hydrazine-1-carbodithioate

methyl (E)-2-(1-(3-((2-methoxyethoxy)methyl)pyridin-2-yl)ethylidene)hydrazine-1-carbodithioate

Conditions
ConditionsYield
In isopropyl alcohol at 60℃;100%
acetylferrocene
1271-55-2

acetylferrocene

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

methyl 2-(1-ferrocenylethylidene)hydrazinecarbodithioate

methyl 2-(1-ferrocenylethylidene)hydrazinecarbodithioate

Conditions
ConditionsYield
With toluene-4-sulfonic acid at 20 - 80℃; for 1.16667h;98.1%
With methanesulfonic acid; choline chloride at 80℃;93.6%
In ethanol addn. of S-methyldithiocarbazate in hot anhydrous ethanol to a soln. of formylferrocene in same solvent; refluxing for 1 h; cooling;; filtration of crystals; washing with cold ethanol; drying in vac.; elem. anal.;;92%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

pyridazine-4-carbaldehyde
50901-42-3

pyridazine-4-carbaldehyde

N'-[1-Pyridazin-4-yl-meth-(E)-ylidene]-hydrazinecarbodithioic acid methyl ester

N'-[1-Pyridazin-4-yl-meth-(E)-ylidene]-hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In isopropyl alcohol at 65 - 70℃; for 1h;98%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

methyl 2-(3-methylpyrazinyl) ketone
23787-80-6

methyl 2-(3-methylpyrazinyl) ketone

methyl 2-[1-(3-methyl-2-pyrazinyl)ethylidene]hydrazinecarbodithioate

methyl 2-[1-(3-methyl-2-pyrazinyl)ethylidene]hydrazinecarbodithioate

Conditions
ConditionsYield
In isopropyl alcohol at 65 - 70℃; for 1h;98%
ferrocenecarboxaldehyde
12093-10-6

ferrocenecarboxaldehyde

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

formylferrocene hydrazinodithioformate methyl ester

formylferrocene hydrazinodithioformate methyl ester

Conditions
ConditionsYield
With toluene-4-sulfonic acid at 20 - 80℃; for 1.08333h;97.5%
In ethanol addn. of S-methyldithiocarbazate in hot anhydrous ethanol to a soln. of formylferrocene in same solvent; refluxing for 1 h; cooling;; filtration of crystals; washing with cold ethanol; drying in vac.; elem. anal.;;96%
In ethanol for 2h; Reflux; Inert atmosphere; Schlenk technique;95%
With methanesulfonic acid; choline chloride at 80℃;91.2%
In isopropyl alcohol Reflux;
1-acetylisoquinoline
58022-21-2

1-acetylisoquinoline

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

methyl 3-<1-(1-isoquinolinyl)ethylidene>hydrazinecarbodithioate
85748-38-5

methyl 3-<1-(1-isoquinolinyl)ethylidene>hydrazinecarbodithioate

Conditions
ConditionsYield
In ethanol for 0.416667h; Heating;97%
9-methyl-9H-carbazole-3-carbaldehyde
21240-56-2

9-methyl-9H-carbazole-3-carbaldehyde

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

C16H15N3S2

C16H15N3S2

Conditions
ConditionsYield
With toluene-4-sulfonic acid at 60℃; for 1.08333h; Green chemistry;96.8%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Methyl 4-pyridazinyl ketone
50901-46-7

Methyl 4-pyridazinyl ketone

N'-[1-Pyridazin-4-yl-eth-(E)-ylidene]-hydrazinecarbodithioic acid methyl ester
124436-43-7

N'-[1-Pyridazin-4-yl-eth-(E)-ylidene]-hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In isopropyl alcohol at 65 - 70℃; for 1h;96%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Oxo-p-tolylamino-dithioacetic acid methyl ester
104688-94-0

Oxo-p-tolylamino-dithioacetic acid methyl ester

5-Methylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid p-tolylamide
104689-05-6

5-Methylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid p-tolylamide

Conditions
ConditionsYield
In ethanol Heating;95%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

1-(5-methylpyrazin-2-yl)ethanone
22047-27-4

1-(5-methylpyrazin-2-yl)ethanone

methyl 2-[1-(5-methyl-2-pyrazinyl)ethylidene]hydrazinecarbodithioate

methyl 2-[1-(5-methyl-2-pyrazinyl)ethylidene]hydrazinecarbodithioate

Conditions
ConditionsYield
In isopropyl alcohol at 65 - 70℃; for 1h;95%
2-pyrrole aldehyde
1003-29-8

2-pyrrole aldehyde

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

[((1E)-1-aza-2-pyrol-2-ylvinyl)amino]phenylmethylthiomethane-1-thione
685567-52-6

[((1E)-1-aza-2-pyrol-2-ylvinyl)amino]phenylmethylthiomethane-1-thione

Conditions
ConditionsYield
In isopropyl alcohol at 20℃; for 2h;95%
Indole-3-carboxaldehyde
487-89-8

Indole-3-carboxaldehyde

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

methyl (E)-2-((1H-indol-3-yl)methylene)hydrazine-1-carbodithioate
685567-53-7

methyl (E)-2-((1H-indol-3-yl)methylene)hydrazine-1-carbodithioate

Conditions
ConditionsYield
In isopropyl alcohol at 20℃; for 2h;95%
cobalt(II) chloride hexahydrate

cobalt(II) chloride hexahydrate

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

Co(3+)*3NH2NC(S)SCH3(1-)=[Co(NH2NC(S)SCH3)3]

Co(3+)*3NH2NC(S)SCH3(1-)=[Co(NH2NC(S)SCH3)3]

Conditions
ConditionsYield
In water 3 equiv. of ligand; elem. anal.;95%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

4-methoxy-5-oxo-5H-furo[3,2-g][1]benzopyran-6-carboxaldehyde

4-methoxy-5-oxo-5H-furo[3,2-g][1]benzopyran-6-carboxaldehyde

C15H12N2O4S2
1131893-26-9

C15H12N2O4S2

Conditions
ConditionsYield
In isopropyl alcohol at 20℃; for 2h;95%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

methyl 4-(6-methylpyrimidinyl) ketone
67073-96-5

methyl 4-(6-methylpyrimidinyl) ketone

methyl 2-[1-(6-methyl-4-pyrimidinyl)ethylidene]hydrazinecarbodithioate

methyl 2-[1-(6-methyl-4-pyrimidinyl)ethylidene]hydrazinecarbodithioate

Conditions
ConditionsYield
In isopropyl alcohol at 65 - 70℃; for 1h;94%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

2-Hydroxy-5-methylisophthalaldehyde
7310-95-4

2-Hydroxy-5-methylisophthalaldehyde

CH3C6H2OH(CHNNHCSSCH3)2
705251-42-9

CH3C6H2OH(CHNNHCSSCH3)2

Conditions
ConditionsYield
In methanol for 4h; Reflux;93.8%
In methanol for 4h; Reflux;93.8%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)benzaldehyde
1181214-29-8

4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)benzaldehyde

(E)-methyl 2-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)benzylidene)hydrazinecarbodithioate
1392735-19-1

(E)-methyl 2-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)benzylidene)hydrazinecarbodithioate

Conditions
ConditionsYield
In ethanol at 80℃; for 3h;93%
In ethanol at 80℃; for 3h;93%
In ethanol at 80℃; for 3h;93%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

trifluoroacetic acid
76-05-1

trifluoroacetic acid

2-(methylthio)-5-(trifluoromethyl)-1,3,4-thiadiazole

2-(methylthio)-5-(trifluoromethyl)-1,3,4-thiadiazole

Conditions
ConditionsYield
In toluene at 10 - 20℃; for 2h;93%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

9-benzyl-9H-carbazole-3-carbaldehyde
54117-37-2

9-benzyl-9H-carbazole-3-carbaldehyde

C22H19N3S2

C22H19N3S2

Conditions
ConditionsYield
With toluene-4-sulfonic acid at 20℃;92.3%
O-methylcaprolactim
2525-16-8

O-methylcaprolactim

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

N'-Azepan-(2E)-ylidene-hydrazinecarbodithioic acid methyl ester
18596-83-3

N'-Azepan-(2E)-ylidene-hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In methanol for 1h; Ambient temperature;92%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

2,2-Dimethoxy-azepane

2,2-Dimethoxy-azepane

N'-Azepan-(2E)-ylidene-hydrazinecarbodithioic acid methyl ester
18596-83-3

N'-Azepan-(2E)-ylidene-hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In methanol for 1h; Ambient temperature;92%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

3-(1-(4-bromophenyl)-5-methyl-1H-1,2,3-triazol-4-yl)-1-phenyl-1H-pyrazole-4 carbaldehyde

3-(1-(4-bromophenyl)-5-methyl-1H-1,2,3-triazol-4-yl)-1-phenyl-1H-pyrazole-4 carbaldehyde

methyl 2-((3-(1-(4-bromophenyl)-5-methyl-1H-1,2,3-triazol-4-yl)-1-phenyl-1H-pyrazol-4-yl)methylene)hydrazine-1-carbodithioate

methyl 2-((3-(1-(4-bromophenyl)-5-methyl-1H-1,2,3-triazol-4-yl)-1-phenyl-1H-pyrazol-4-yl)methylene)hydrazine-1-carbodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃;92%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

9-butyl-9H-carbazole-3-carbaldehyde
67707-09-9

9-butyl-9H-carbazole-3-carbaldehyde

C19H21N3S2

C19H21N3S2

Conditions
ConditionsYield
With toluene-4-sulfonic acid at 20℃;92%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

1-(pyridazin-3-yl)ethan-1-one
1122-63-0

1-(pyridazin-3-yl)ethan-1-one

N'-[1-Pyridazin-3-yl-eth-(E)-ylidene]-hydrazinecarbodithioic acid methyl ester
124436-48-2

N'-[1-Pyridazin-3-yl-eth-(E)-ylidene]-hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In isopropyl alcohol at 65 - 70℃; for 1h;91%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

6-acetyl-4H-benzo[1,4]oxazin-3-one
26518-71-8

6-acetyl-4H-benzo[1,4]oxazin-3-one

Methyl 3-<(3-oxo-2H,1,4-benzoxazin-6-yl)-ethylidene>hydrazinecarbodithioate
113769-59-8

Methyl 3-<(3-oxo-2H,1,4-benzoxazin-6-yl)-ethylidene>hydrazinecarbodithioate

Conditions
ConditionsYield
With acetic acid In ethanol for 1h; Heating;91%
formaldehyd
50-00-0

formaldehyd

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

4-methoxyphenylboronic acid
5720-07-0

4-methoxyphenylboronic acid

3-(4-methoxybenzyl)-5-(methylthio)-2,3-dihydro-1,3,4-thiadiazole

3-(4-methoxybenzyl)-5-(methylthio)-2,3-dihydro-1,3,4-thiadiazole

Conditions
ConditionsYield
In dichloromethane; water at 60℃; for 12h; Sealed tube;91%
1-acetyl-1H-indole-2,3-dione
574-17-4

1-acetyl-1H-indole-2,3-dione

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

S-methyl ester of 1-acetylisatin 3-dithiocarboxyhydrazone
78344-53-3

S-methyl ester of 1-acetylisatin 3-dithiocarboxyhydrazone

Conditions
ConditionsYield
With acetic acid for 1h;90.3%
hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

salicylaldehyde
90-02-8

salicylaldehyde

methyl 2-(2-hydroxybenzylidene)hydrazinecarbodithioate
133978-98-0, 26151-73-5

methyl 2-(2-hydroxybenzylidene)hydrazinecarbodithioate

Conditions
ConditionsYield
In ethanol90%
In ethanol for 12h; Reflux;68%
In methanol Reflux;61%

Methyldithiocarbazate Specification

The Methyldithiocarbazate is an organic compound with the formula C2H6N2S2. The IUPAC name of this chemical is methyl N-aminocarbamodithioate. With the CAS registry number 5397-03-5, it is also named as Dithiocarbazic acid methyl ester. The classification codes are TSCA Flag P [A commenced PMN (Premanufacture Notice) substance]; 
TSCA Flag S [Substance is identified in a proposed or final SNUR (Significant New Use Rule) under TSCA]. In addition, the molecular weight is 122.21.

The other characteristics of this product can be summarized as: (1)ACD/LogP: 0.39; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.39; (4)ACD/LogD (pH 7.4): 0.38; (5)ACD/BCF (pH 5.5): 1.17; (6)ACD/BCF (pH 7.4): 1.15; (7)ACD/KOC (pH 5.5): 38.89; (8)ACD/KOC (pH 7.4): 38.23; (9)#H bond acceptors: 2; (10)#H bond donors: 3; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 63.87 Å2; (13)Index of Refraction: 1.645; (14)Molar Refractivity: 33.73 cm3; (15)Molar Volume: 92.9 cm3; (16)Polarizability: 13.37×10-24 cm3; (17)Surface Tension: 66.8 dyne/cm; (18)Density: 1.314 g/cm3; (19)Flash Point: 79.2 °C; (20)Enthalpy of Vaporization: 44.36 kJ/mol; (21)Boiling Point: 207.3 °C at 760 mmHg; (22)Vapour Pressure: 0.227 mmHg at 25°C.

Uses of Methyldithiocarbazate: It can react with furfural to get furfurylidene-hydrazinecarbodithioic acid methyl ester. This reaction which is a kind of condensation needs solvent ethanol by heating. The reaction time is 1 hours. The yield is 50%.

Methyldithiocarbazate can react with furfural to get furfurylidene-hydrazinecarbodithioic acid methyl ester

People can use the following data to convert to the molecule structure. 
1. SMILES:S=C(SC)NN
2. InChI:InChI=1/C2H6N2S2/c1-6-2(5)4-3/h3H2,1H3,(H,4,5)
3. InChIKey:ILAXBOIRSPXAMM-UHFFFAOYAV

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