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31898-49-4

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31898-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31898-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,8,9 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 31898-49:
(7*3)+(6*1)+(5*8)+(4*9)+(3*8)+(2*4)+(1*9)=144
144 % 10 = 4
So 31898-49-4 is a valid CAS Registry Number.

31898-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1,1-dioxo-1,4-thiazinan-4-yl)-1-[2-(5-nitrofuran-2-yl)-1,3-thiazol-4-yl]methanimine

1.2 Other means of identification

Product number -
Other names Acetonitrile,[(1,1-dioxido-1,2-benzisothiazol-3-yl)thio]

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:31898-49-4 SDS

31898-49-4Downstream Products

31898-49-4Relevant articles and documents

Antiprotozoal thiazoles. 2. 2 (5 Nitro 2 furyl-, thiazolyl-, and 1 methylimidazolyl-)thiazoles

Neville,Verge

, p. 946 - 949 (2007/10/08)

Ten 2 substituted 4 thiazolecarboxaldehyde hydrazones bearing 5 nitro 2 furyl, 5 nitro 2 thiazolyl, and 1 methyl 5 nitro 2 imidazolyl functions have been prepared and screened for activity against Trypanosoma cruzi infections in mice. The results permitted the ranking of these substituents in decreasing order of activity: 1 methyl 5 nitro 2 imidazolyl > 5 nitro 2 furyl > 5 nitro 2 thiazolyl, the last being inactive. Some structural features of the side chain necessary for optimum activity are discussed. The most active compound, 4 [[[2 (1 methyl 5 nitro 2 imidazolyl) 4 thiazolyl]methylene]amino]thiomorpholine 1,1 dioxide, compared favorably with the standard Nifurtimox against 3 recent clinical isolates of T. cruzi, including 1 with a high myocardial tissue infiltration.

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