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Merck
CN

264989

2-Methyl-3-thiosemicarbazide

97%

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About This Item

Linear Formula:
H2NCSN(CH3)NH2
CAS Number:
Molecular Weight:
105.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
230-071-5
MDL number:
Assay:
97%
Form:
powder
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Quality Level

assay

97%

form

powder

mp

173-175 °C (lit.)

SMILES string

CN(N)C(N)=S

InChI

1S/C2H7N3S/c1-5(4)2(3)6/h4H2,1H3,(H2,3,6)

InChI key

IIGQLQZSWDUOBI-UHFFFAOYSA-N

General description

The rate constant for dihydroxy intermediate formation from 2-methyl-3-thiosemicarbazide was studied.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Synthesis and characterization of new amino acyl-4-thiazolidones.
Leite ACL, et al.
Quimica nova, 30(2), 284-286 (2007)
Franco Bisceglie et al.
Metallomics : integrated biometal science, 8(12), 1255-1265 (2016-11-15)
A comparative study between two bisthiosemicarbazones, 2,3-butanedione bis(4,4-dimethyl-3-thiosemicarbazone) and 2,3-butanedione bis(2-methyl-3-thiosemicarbazone), and their copper(ii) complexes is reported. The four compounds have been tested on a leukemia cell line U937 (p53-null) and on an adenocarcinoma cell line A549. The study includes
Reaction between various benzaldehydes and phenylhydroxylamine: special behaviour compared with other amines.
Brighente IM, et al.
J. Chem. Soc. Perkin Trans. II, 11, 1861-1864 (1991)



Global Trade Item Number

SKUGTIN
264989-1G04061826198100