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18667-57-7

pentane-2,3-dione dithiosemicarbazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 18667-57-7 Structure

  • Basic information

    1. Product Name: pentane-2,3-dione dithiosemicarbazone
    2. Synonyms:
    3. CAS NO:18667-57-7
    4. Molecular Formula: C7H14N6S2
    5. Molecular Weight: 246.3563
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 18667-57-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 399.2°C at 760 mmHg
    3. Flash Point: 195.3°C
    4. Appearance: N/A
    5. Density: 1.42g/cm3
    6. Vapor Pressure: 1.39E-06mmHg at 25°C
    7. Refractive Index: 1.674
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: pentane-2,3-dione dithiosemicarbazone(CAS DataBase Reference)
    11. NIST Chemistry Reference: pentane-2,3-dione dithiosemicarbazone(18667-57-7)
    12. EPA Substance Registry System: pentane-2,3-dione dithiosemicarbazone(18667-57-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 18667-57-7(Hazardous Substances Data)

18667-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18667-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,6 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18667-57:
(7*1)+(6*8)+(5*6)+(4*6)+(3*7)+(2*5)+(1*7)=147
147 % 10 = 7
So 18667-57-7 is a valid CAS Registry Number.

18667-57-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(Z)-[(2E)-2-(carbamothioylhydrazinylidene)pentan-3-ylidene]amino]thiourea

1.2 Other means of identification

Product number -
Other names Methyl-ethylglyoxal-dithiosemicarbazon

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18667-57-7 SDS

18667-57-7Downstream Products

18667-57-7Relevant articles and documents

Identification of differential anti-neoplastic activity of copper bis(thiosemicarbazones) that is mediated by intracellular reactive oxygen species generation and lysosomal membrane permeabilization

Stefani, Christian,Al-Eisawi, Zaynab,Jansson, Patric J.,Kalinowski, Danuta S.,Richardson, Des R.

, p. 20 - 37 (2015)

Bis(thiosemicarbazones) and their copper (Cu) complexes possess unique anti-neoplastic properties. However, their mechanism of action remains unclear. We examined the structure-activity relationships of twelve bis(thiosemicarbazones) to elucidate factors

Synthesis and Characterisation of Indium(III) Bis-Thiosemicarbazone Complexes: 18F Incorporation for PET Imaging

Venkatachalam, Taracad K.,Bernhardt, Paul V.,Pierens, Gregory K.,Stimson, Damion H. R.,Bhalla, Rajiv,Reutens, David C.

, p. 383 - 391 (2019/03/21)

Several structurally related indium chlorido complexes of bis-thiosemicarbazones were prepared, starting from the appropriately substituted bis-thiosemicarbazones, using sodium methoxide in methanol. Detailed NMR studies were conducted to assign the struc

IMAGING AGENTS

-

Paragraph 0088, (2017/05/17)

The present invention provides certain thiosemicarbazone metal complexes which have advantageous properties in medical imaging. The thiosemicarbazone metal complexes can be safely and easily produced in real time, administered quickly after production, readily cross the blood-brain barrier, and may utilize a number of different radionuclides.

Heteronuclear NMR Spectroscopic Investigations of Gallium Complexes of Substituted Thiosemicarbazones Including X-Ray Crystal Structure, a New Halogen Exchange Strategy, and 18F Radiolabelling

Venkatachalam,Pierens,Bernhardt, Paul V.,Stimson,Bhalla,Lambert,Reutens

, p. 1033 - 1048 (2016/10/12)

Five thiosemicarbazone ligands have been synthesized, and their coordination chemistry with gallium was investigated. The reaction of these thiosemicarbazones with gallium chloride in alcohol solutions in the presence of a base yielded the corresponding p

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