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1,2,4-Triazin-5(2H)-one, 6-phenyl-3-(2-propenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87450-65-5

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87450-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87450-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,5 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87450-65:
(7*8)+(6*7)+(5*4)+(4*5)+(3*0)+(2*6)+(1*5)=155
155 % 10 = 5
So 87450-65-5 is a valid CAS Registry Number.

87450-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(allythio)-6-phenyl-1,2,4-triazin-5(2H)-one

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:87450-65-5 SDS

87450-65-5Relevant academic research and scientific papers

NEW SUBSTITUTED AZATHYMIDINE DERIVATIVES AND THEIR USE IN THE TREATMENT OF BACTERIAL INFECTIOUS DISEASES

-

Page/Page column 43; 48, (2008/06/13)

The invention relates to substituted azathymidines and related compounds of formula (I), wherein X is N or CH, and R1, R2 and R3 are as described in the specification, processes for the preparation thereof, pharmaceutical compositions containing the same, the use thereof optionally in combination with one or more other pharmaceutically active compounds as antibacterial agents for the therapy of infective diseases, and a method for the treatment of such diseases. The compounds of formula (I) are reducing selectively the pathogenicity of bacteria within the host, but without affecting the bacteria outside the host environment.

Palladium-Catalyzed Polyhetero-Claisen Rearragement of 3-(Allylthio)-1,2,4-triazin-5(4H)-ones

Mizutani, Masato,Sanemitsu, Yuzuru,Tamaru, Yoshinao,Yoshida, Zen-ichi

, p. 4585 - 4589 (2007/10/02)

The S -> N allylic transposition of 3-(allylthio)-1,2,4-triazin-5(2H)-ones (2) has been performed successfully by catalysis of a palladium(II) salt, where regioselectivities of the rearrangement (N-2 vs.N-4) are highly dependent on the substitution patter

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