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N-(p-Nitrobenzoyl)thiazolidine-2-thione is a chemical compound with the molecular formula C10H8N2O3S2. It is a derivative of thiazolidine-2-thione, featuring a p-nitrobenzoyl group attached to the nitrogen atom. This yellow crystalline solid is soluble in organic solvents and is commonly used as a reagent in organic synthesis, particularly for the preparation of various heterocyclic compounds and as a protecting group in peptide synthesis. Its chemical structure and properties make it a valuable tool in the field of chemistry, allowing for the creation of complex molecules and the study of their reactions.

1438-01-3

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1438-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1438-01-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1438-01:
(6*1)+(5*4)+(4*3)+(3*8)+(2*0)+(1*1)=63
63 % 10 = 3
So 1438-01-3 is a valid CAS Registry Number.

1438-01-3SDS

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 (4-Nitrophenyl)(2-thioxo-1,3-thiazolidin-3-yl)methanone

1.2 Other means of identification

Product number -
Other names 3-p-Nitrobenzoyloxazolidin-2-on

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:1438-01-3 SDS

1438-01-3Relevant academic research and scientific papers

NOUVEAUX DECONTAMINANTS GENERATION "IN SITU" D'UN PERACIDE PAR ACTION D'UN PERSEL SUR UN INITIATEUR, REACTIVITE DE CE PERACIDE VIS-A-VIS DU PARAOXON

Lion, Claude,Hedayatullah, Mir,Charvy, Claude,Briand, Sylvette,Vincent, Stephane,et al.

, p. 515 - 520 (2007/10/02)

The formation of peroxyacids by the reaction of a persalt (sodium percarbonate, sodium perborate,...) with an initiator (TAED, TAGU, NOBS, ISNOBS, PAG, acylsugars) has been developed.The reactivity of these peroxyacids generated "in situ" has been studied in the destruction of paraoxon (O,O-diethyl O-paranitrophenylphosphate) with some long chain tetraalkylammonium salts.

SUGAR CHEMISTRY WITHOUT PROTECTING GROUPS-III. A FACILE CHEMICAL SYNTHESIS OF 6-O-ACYL-D-GLYCOPYRANOSES AND METHYL-6-O-ACYL-D-GLYCOPYRANOSIDES.

Baczko, Krystyna,Plusquellec, Daniel

, p. 3817 - 3828 (2007/10/02)

Regioselective acylation of non protected glycopyranosides was performed using 3-acylthiazolidine-2-thiones 1 and the novel 3-acyl-5-methyl-1,3,4-thiadiazole-2(3H)-thiones 2 as the acylating reagents, yielding 6-O-acylated derivatives in high yields.Acyla

Radiosensitizing nitrobenzoic acid amide derivatives

-

, (2008/06/13)

Nitrobenzoic acid amide derivative represented by the formula STR1 wherein A is (CH2)x NH(CH2)y or (CH2)x NH(CH2)y NH(CH2)z, n is 1 or 2, x, y an

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