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CAS

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5426-05-1

Ethyl (1E)-ethanimidothioate, also known as ethyl thioacetamidate or ethyl 2-iminoacetate, is an organic compound with the chemical formula C4H9NS. It is a colorless liquid with a pungent odor and is soluble in water. ethyl (1E)-ethanimidothioate is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other chemical products. It is synthesized by the reaction of ethyl acetate with hydrogen sulfide and ammonia. Ethyl (1E)-ethanimidothioate is an important building block in the synthesis of various heterocyclic compounds and has applications in the fields of organic chemistry and medicinal chemistry.

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  • 5426-05-1 Structure

  • Basic information

    1. Product Name: ethyl (1E)-ethanimidothioate
    2. Synonyms:
    3. CAS NO:5426-05-1
    4. Molecular Formula: C4H9NS*ClH
    5. Molecular Weight: 103.186
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5426-05-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 117°C at 760 mmHg
    3. Flash Point: 24.5°C
    4. Appearance: N/A
    5. Density: 0.97g/cm3
    6. Vapor Pressure: 21.2mmHg at 25°C
    7. Refractive Index: 1.484
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ethyl (1E)-ethanimidothioate(CAS DataBase Reference)
    11. NIST Chemistry Reference: ethyl (1E)-ethanimidothioate(5426-05-1)
    12. EPA Substance Registry System: ethyl (1E)-ethanimidothioate(5426-05-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5426-05-1(Hazardous Substances Data)

5426-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5426-05-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5426-05:
(6*5)+(5*4)+(4*2)+(3*6)+(2*0)+(1*5)=81
81 % 10 = 1
So 5426-05-1 is a valid CAS Registry Number.

5426-05-1SDS

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 ethyl ethanimidothioate,hydrochloride

1.2 Other means of identification

Product number -
Other names thioacetimidic acid ethyl ester,hydrochloride

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:5426-05-1 SDS

5426-05-1Relevant articles and documents

Syntheses, characterization and biological activities of two carbamate pesticides

Bansal

, p. 968 - 971 (2007/10/03)

Two carbamate pesticides namely S-ethyl-N-[(methylcarbamoyl)oxy] thioacetimidate (a) (CH3-C|SC2H5=NOCONHCH3) and N-phenyl-(ethylcarbamoyl)propyl carbamate (b) [C6H 5NH-COO-CH(CH3)-CO-NH(Cs

2-β-D-RIBOFURANOSYLBENZOXAZOLE FROM 2,5-ANHYDRO-D-ALLONOIMIDATE, AND 1,3-DIMETHYL-8-β-D-RIBOFURANOSYLXANTHINE FROM 2,5-ANHYDRO-D-ALLONO-THIOIMIDATES AND -DITHIOATES

Khadem, Hassan S. El,Kawai, Joshua

, p. 271 - 284 (2007/10/02)

The ability of imidates, thioimidates, and dithioates to react with o-aminophenol (2) and 5,6-diamino-1,3-dimethyluracil (6) was studied, using nonsaccharide model compounds, as well as saccharide derivatives.All of the model compounds gave 2-methylbenzoxazole, but only ethyl dithioacetate gave a purine derivative with 6.Methyl 2,5-anhydro-D-allonoimidate hydrochloride reacted with 2 to yield 2-β-D-ribofuranosylbenzoxazole, but failed to react with compound 6.On reaction with compound 6 such fully acylated thioimidates as ethyl and benzyl 2,5-anhydrotri-O-benzoyl- or tri-O-p-toluoyl-D-allonothioimidate hydrochloride yielded amidines that underwent aromatization of the furanose ring.Such monoacylated thioimidates as ethyl or benzyl 2,5-anhydro-6-O-benzoyl-D-allonothioimidate hydrochloride yielded, with compound 6, 8-(5-O-benzoyl-β-D-ribofuranosyl)-1,3-dimethylxanthine, without aromatization.Such dithioates as benzyl 2,5-anhydro-6-O-benzoyl-D-allonodithioate and ethyl 2,5-anhydrotri-O-benzoyl-D-allonodithioate were obtained by treating the corresponding thioimidate with H2S in pyridine.With compound 6, the first yielded 8-(5-O-benzoyl-β-D-ribofuranosyl)-1,3-dimethylxanthine, which afforded the free C-nucleoside 1,3-dimethyl-8-β-D-ribofuranosylxanthine on treatment with methanolic ammonia.

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