What is the [[(diethylamino)thioxomethyl]thio]acetic acid?

[[(diethylamino)thioxomethyl]thio]acetic acid is , while it's Molecular Formula is C7H13 N O2 S2. Used in Organic Synthesis: [[(diethylamino)thioxomethyl]thio]acetic acid is used as a building block in organic synthesis for its ability to participate in various chemical reactions due to the presence of the thioxo and diethylamino groups. This allows for the creation of a wide range of new compounds with different properties and applications. Used in Pharmaceutical Research: In the pharmaceutical industry, [[(diethylamino)thioxomethyl]thio]acetic acid is utilized as a key intermediate in the development of new drugs. Its unique structure and functional groups make it a promising candidate for the synthesis of bioactive molecules with potential therapeutic effects. Used in the Development of New Materials: [[(diethylamino)thioxomethyl]thio]acetic acid's properties also make it valuable in the development of new materials with specific characteristics. For instance, its sulfur-containing structure can contribute to the formation of materials with unique electronic, optical, or mechanical properties, depending on the nature of the reactions and the resulting compounds.

What is the CAS number for [[(diethylamino)thioxomethyl]thio]acetic acid?

The CAS number of [[(diethylamino)thioxomethyl]thio]acetic acid is 5439-93-0.

What is the [[(diethylamino)thioxomethyl]thio]acetic acid?

[[(diethylamino)thioxomethyl]thio]acetic acid is , while it's Molecular Formula is C7H13 N O2 S2. Used in Organic Synthesis: [[(diethylamino)thioxomethyl]thio]acetic acid is used as a building block in organic synthesis for its ability to participate in various chemical reactions due to the presence of the thioxo and diethylamino groups. This allows for the creation of a wide range of new compounds with different properties and applications. Used in Pharmaceutical Research: In the pharmaceutical industry, [[(diethylamino)thioxomethyl]thio]acetic acid is utilized as a key intermediate in the development of new drugs. Its unique structure and functional groups make it a promising candidate for the synthesis of bioactive molecules with potential therapeutic effects. Used in the Development of New Materials: [[(diethylamino)thioxomethyl]thio]acetic acid's properties also make it valuable in the development of new materials with specific characteristics. For instance, its sulfur-containing structure can contribute to the formation of materials with unique electronic, optical, or mechanical properties, depending on the nature of the reactions and the resulting compounds.

What is the CAS number for [[(diethylamino)thioxomethyl]thio]acetic acid?

The CAS number of [[(diethylamino)thioxomethyl]thio]acetic acid is 5439-93-0.

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[[(diethylamino)thioxomethyl]thio]acetic acid

Q: What is [[(diethylamino)thioxomethyl]thio]acetic acid (5439-93-0) used for?

[[(diethylamino)thioxomethyl]thio]acetic acid is a sulfur-containing organic molecule characterized by the presence of a thioxo group, which is a functional group composed of a sulfur atom double-bonded to an oxygen atom, and a diethylamino group, consisting of two ethyl groups attached to an amino group. The unique combination of these functional groups endows the compound with potential for diverse chemical reactions and applications, making it a valuable tool in organic synthesis and pharmaceutical research for the development of new materials and compounds.InChI:InChI=1/C7H13NO2S2/c1-3-8(4-2)7(11)12-5-6(9)10/h3-5H2,1-2H3,(H,9,10)

Basic Information

CAS No.:5439-93-0
Purity:99%

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Details

Factory Sells Best Quality [[(diethylamino)thioxomethyl]thio]acetic acid 5439-93-0 with stock

Molecular Formula:C7H13 N O2 S2
Molecular Weight:207.318
Vapor Pressure:6.74E-05mmHg at 25°C
Boiling Point:320.2°Cat760mmHg
Flash Point:147.4°C
PSA：97.93000
Density:1.257g/cm³
LogP:1.43090

[[(diethylamino)thioxomethyl]thio]acetic acid(Cas 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.

InChI:InChI=1/C7H13NO2S2/c1-3-8(4-2)7(11)12-5-6(9)10/h3-5H2,1-2H3,(H,9,10)

5439-93-0 Relevant articles

Synthesis, characterization and biological evaluation of novel 1-N-substituted thiocarbomoyl-3-ferrocenyl-2-pyrazoline derivatives

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, p. 1835 - 1840 (2016/07/06)

Some novel 1-N-substituted thiocarbomoyl...

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

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Protein recognition polymers capable of ...

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 prep...

Synthesis of a new series of dithiocarbamate-linked peptidomimetics and their application in Ugi reactions

Ziyaei Halimehjani, Azim,Ranjbari, Mohammad Amin,Pasha Zanussi, Hamed

, p. 22904 - 22908 (2013/11/19)

Novel peptidomimetics containing dithioc...

5439-93-0 Process route

: 3926-62-3
sodium monochloroacetic acid

: 148-18-5
sodium N,N-diethyldithiocarbamate

: 5439-93-0
(N,N-diethylthiocarbamoylthio)acetic acid

Conditions

Conditions	Yield
With hydrogenchloride; In water; benzene; at 70 ℃; for 5h;	86%
With water; at 20 ℃; Darkness;	50%

In water; at 20 ℃; for 48h; Darkness;

: 75-15-0,12122-00-8
carbon disulfide

: 3926-62-3
sodium monochloroacetic acid

: 109-89-7
diethylamine

: 5439-93-0
(N,N-diethylthiocarbamoylthio)acetic acid

Conditions

Conditions	Yield
carbon disulfide; sodium monochloroacetic acid; diethylamine; With potassium hydroxide; With hydrogenchloride;
With potassium hydroxide; In ethanol; water; at 20 ℃;
carbon disulfide; diethylamine; With sodium hydroxide; for 4h; sodium monochloroacetic acid; at 20 ℃; With hydrogenchloride; In water;

5439-93-0 Upstream products

3926-62-3
sodium monochloroacetic acid
148-18-5
sodium N,N-diethyldithiocarbamate
3699-30-7
potassium diethyldithiocarbamate
75-15-0
carbon disulfide

5439-93-0 Downstream products

21198-48-1
4,4-diethyl-thiosemicarbazide
51661-15-5
S-<(N-phenylcarbamoyl)methyl> diethyldithiocarbamate
107348-00-5
Diethyl-dithiocarbamic acid benzylcarbamoyl-methyl ester
107348-01-6
Diethyl-dithiocarbamic acid (methyl-phenyl-carbamoyl)-methyl ester

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