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5439-93-0

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5439-93-0 Usage

General Description

The chemical compound [(diethylamino)thioxomethyl]thio]acetic acid is a sulfur-containing organic molecule. It contains a thioxo group, which is a functional group composed of a sulfur atom double-bonded to an oxygen atom. The compound also contains a diethylamino group, which consists of two ethyl groups attached to an amino group. The presence of both thioxo and diethylamino groups in the molecule gives it potential for various chemical reactions and applications. It is used in organic synthesis and pharmaceutical research, and its properties make it a valuable tool in the development of new materials and compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 5439-93-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5439-93:
(6*5)+(5*4)+(4*3)+(3*9)+(2*9)+(1*3)=110
110 % 10 = 0
So 5439-93-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO2S2/c1-3-8(4-2)7(11)12-5-6(9)10/h3-5H2,1-2H3,(H,9,10)

5439-93-0SDS

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 2-(diethylcarbamothioylsulfanyl)acetic acid

1.2 Other means of identification

Product number -
Other names diethyldithiocarbamylacetic acid

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:5439-93-0 SDS

5439-93-0Relevant articles and documents

Gottstein et al.

, p. 1693 (1970)

Fluorescent protein-imprinted polymers capable of signal transduction of specific binding events prepared by a site-directed two-step post-imprinting modification

Sunayama, Hirobumi,Ooya, Tooru,Takeuchi, Toshifumi

supporting information, p. 1347 - 1349 (2014/01/23)

Protein recognition polymers capable of highly specific transduction of protein binding events into fluorescence change were prepared by molecular imprinting in conjunction with a newly developed two-step post-imprinting chemical modification of functional groups located within the protein recognition cavity. The Royal Society of Chemistry.

Molecularly imprinted polymers prepared using protein-conjugated cleavable monomers followed by site-specific post-imprinting introduction of fluorescent reporter molecules

Suga, Yusuke,Sunayama, Hirobumi,Ooya, Tooru,Takeuchi, Toshifumi

supporting information, p. 8450 - 8452 (2013/09/23)

Molecularly imprinted polymers were prepared using a protein-conjugated disulfide cleavable monomer. After removing the protein by disulfide reduction, a thiol-reactive fluorophore was introduced into the thiol residue located only inside the imprinted cavity, resulting in specific transduction of the binding events into fluorescence spectral change. The Royal Society of Chemistry 2013.

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