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Merck
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Key Documents

264989

Sigma-Aldrich

2-甲基氨基硫脲

97%

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About This Item

線性公式:
H2NCSN(CH3)NH2
CAS號碼:
分子量::
105.16
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

形狀

powder

mp

173-175 °C (lit.)

SMILES 字串

CN(N)C(N)=S

InChI

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

InChI 密鑰

IIGQLQZSWDUOBI-UHFFFAOYSA-N

一般說明

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析證明 (COA)

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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)
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

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