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Pentanedioic acid, 2-[dihydro-5-(phenylmethyl)-6-thioxo-2H-1,3,5-thiadiazin-3(4H)-yl]-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138995-93-4

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138995-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138995-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,9 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138995-93:
(8*1)+(7*3)+(6*8)+(5*9)+(4*9)+(3*5)+(2*9)+(1*3)=194
194 % 10 = 4
So 138995-93-4 is a valid CAS Registry Number.

138995-93-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-Benzyl-6-thioxo-[1,3,5]thiadiazinan-3-yl)-pentanedioic acid

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:138995-93-4 SDS

138995-93-4Downstream Products

138995-93-4Relevant academic research and scientific papers

Synthesis and antifungal activities of some new tetrahydro-2H-1,3,5-thiadiazine-2-thiones

Ertan,Ayyildiz,Yulug

, p. 1182 - 1185 (2007/10/02)

A number of new 3-benzyl-5-[α-(substituted)carboxymethyl]-tetrahydro-2H- 1,3,5-thiadiazine-2-thiones has been synthesized as prodrugs by incorporating the amine group of some amino acid into tetrahydro-2H-1,3,5-thiadiazine-2-thione ring. The compounds have been prepared by the reactions of benzylamine with potassium hydroxide, carbon disulphide formaldehyde and various amino acids. The structures of the compounds have been elucidated by UV, IR, 1H-NMR, mass spectra and elementary analysis. The in vitro activity of these compounds against yeast-like fungi (Candida albicans, C. parapsilosis, C. pseudotropicalis, C. stellatoidea) was investigated by tube dilution method. Their minimal inhibitory concentration (MIC) and minimal fungicidal concentration (MFC) values were determined. All the compounds were found to be active between 3.12- 12.5 μg/ml against the four fungi tested.

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