358851

Sigma-Aldrich

Ethyl dithioacetate

98%

Linear Formula:
CH3CSSCH2CH3
CAS Number:
Molecular Weight:
120.24
Beilstein/REAXYS Number:
1737711
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

assay

98%

refractive index

n20/D 1.568 (lit.)

bp

61 °C/23 mmHg (lit.)

density

1.048 g/mL at 25 °C (lit.)

SMILES string

CCSC(C)=S

InChI

1S/C4H8S2/c1-3-6-4(2)5/h3H2,1-2H3

InChI key

KCOPWUJJPSTRIZ-UHFFFAOYSA-N

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General description

Ethyl dithioacetate is an alkyl dithioester. It reacts with 5,6-diamino-1,3-dimethyluracil to yield the purine derivative. Raman spectra of ethyl dithioacetate has been recorded as a function of temperature in the liquid phase and in the solid phase at low temperature.

Application

Ethyl dithioacetate may be used in the preparation of N-thioacetylamino acids.

Packaging

1, 5 mL in glass bottle

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Target Organs

Respiratory system

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

UN 3272 3 / PGIII

WGK Germany

WGK 3

Flash Point(F)

114.8 °F - closed cup

Flash Point(C)

46 °C - closed cup

2-?-d-ribofuranosylbenzoxazole from 2, 5-anhydro-d-allonoimidate, and 1, 3-dimethyl-8-?-d-ribofuranosylxanthine from 2, 5-anhydro-d-allono-thioimidates and-dithioates.
El Khadem HS and Kawai J.
Carbohydrate Research, 153(2), 271-283 (1986)
Rotational isomers of ethyl dithioacetate and ethyl thionoacetate: A Raman study.
Verma AL, et al.
Journal of Raman Spectroscopy, 11(5), 390-392 (1981)
Thioacetylation method of protein sequencing: Gas chromatography/Ion trap mass spectrometric detection of 5-acetoxy-2-methylthiazoles.
Stolowitz ML, et al.
Journal of Protein Chemistry, 11(4), 360-361 (1992)
Renwu Li et al.
Bioorganic & medicinal chemistry, 28(7), 115356-115356 (2020-02-19)
Past few years have seen an active pursuit of the inhibitors for the deacylation catalyzed by the seven human sirtuins (i.e. SIRT1-7) as valuable chemical biological/pharmacological probes of this enzymatic deacylation and lead compounds for developing novel therapeutics for human...

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