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ammonium 2,3-dimethylphenyl dithiocarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108654-37-1

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108654-37-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108654-37-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,5 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108654-37:
(8*1)+(7*0)+(6*8)+(5*6)+(4*5)+(3*4)+(2*3)+(1*7)=131
131 % 10 = 1
So 108654-37-1 is a valid CAS Registry Number.

108654-37-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ammonium 2,3-dimethylphenyl dithiocarbamate

1.2 Other means of identification

Product number -
Other names -

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:108654-37-1 SDS

108654-37-1Relevant academic research and scientific papers

Synthesis and biological activities of novel artemisinin derivatives as cysteine protease falcipain-2 inhibitors

Liu, Yang,Lu, Wei-Qiang,Cui, Kun-Qiang,Luo, Wei,Wang, Jian,Guo, Chun

, p. 1525 - 1531 (2013/03/14)

A series of novel artemisinin derivatives were synthesized from artemisinin and different anilines. All compounds were obtained as β-isomers. The target compounds were evaluated for inhibition activity against Plasmodium falciparum falcipain-2 in vitro, and most of them exhibited potent inhibition in the low micromolar range and proved to be new types of falcipain-2 inhibitors.

Synthesis, antioxidant activities and urease inhibition of some new 1,2,4-triazole and 1,3,4-thiadiazole derivatives

Khan, Imtiaz,Ali, Sajid,Hameed, Shahid,Rama, Nasim Hasan,Hussain, Muhammad Tahir,Wadood, Abdul,Uddin, Reaz,Ul-Haq, Zaheer,Khan, Ajmal,Ali, Sajjad,Choudhary, M. Iqbal

scheme or table, p. 5200 - 5207 (2011/01/04)

New series of 4,5-disubstituted-2,4-dihydro-3H-1,2,4-triazole-3-thiones (8a-j) and 2,5-disubstituted-1,3,4-thiadiazoles (9a-h) were synthesized by dehydrative cyclization of hydrazinecarbothioamide derivatives (7a-k) by refluxing in 4 N aqueous sodium hydroxide and by overnight stirring with polyphosphoric acid, respectively. The structures of the newly synthesized compounds were characterized by IR, 1H NMR, 13C NMR, elemental analysis and mass spectroscopic studies and the synthesized compounds were screened for their antioxidant and urease inhibition activities. N-(2,4-Dimethylphenyl)-5-(4-nitrophenyl)-1,3,4-thiadiazol-2-amine (9h) showed excellent antioxidant activity more than the standard drug whereas 4-(2,4-dimethylphenyl)-5-(3-nitrophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (8d) and 4-(2,3-dimethylphenyl)-5-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-thione (8e) exhibited potent urease inhibitory activities.

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