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N-[BIS(METHYLTHIO)METHYLENE]GLYCINE ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54985-61-4 Structure
  • Basic information

    1. Product Name: N-[BIS(METHYLTHIO)METHYLENE]GLYCINE ETHYL ESTER
    2. Synonyms: N-[BIS(METHYLTHIO)METHYLENE]GLYCINE ETHYL ESTER;ETHYL 2-(BIS(METHYLTHIO)METHYLENEAMINO)ACETATE
    3. CAS NO:54985-61-4
    4. Molecular Formula: C7H13NO2S2
    5. Molecular Weight: 207.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54985-61-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 276.289°C at 760 mmHg
    3. Flash Point: 120.895°C
    4. Appearance: /
    5. Density: 1.151g/cm3
    6. Vapor Pressure: 0.005mmHg at 25°C
    7. Refractive Index: 1.525
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-[BIS(METHYLTHIO)METHYLENE]GLYCINE ETHYL ESTER(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-[BIS(METHYLTHIO)METHYLENE]GLYCINE ETHYL ESTER(54985-61-4)
    12. EPA Substance Registry System: N-[BIS(METHYLTHIO)METHYLENE]GLYCINE ETHYL ESTER(54985-61-4)
  • 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: 54985-61-4(Hazardous Substances Data)

54985-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54985-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,8 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54985-61:
(7*5)+(6*4)+(5*9)+(4*8)+(3*5)+(2*6)+(1*1)=164
164 % 10 = 4
So 54985-61-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO2S2/c1-4-10-6(9)5-8-7(11-2)12-3/h4-5H2,1-3H3

54985-61-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[bis(methylsulfanyl)methylideneamino]acetate

1.2 Other means of identification

Product number -
Other names N-(ethoxycarbonylmethyl)iminodithiocarbonate

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:54985-61-4 SDS

54985-61-4Relevant articles and documents

Synthesis, cytotoxic activity, DNA binding and molecular docking studies of novel 9-anilinothiazolo[5,4-b]quinoline derivatives

Reyes-Rangel, Francisco J.,López-Rodríguez, A. Kémish,Pastrana-Cancino, Laura V.,Loza-Mejía, Marco. A.,Solano, José D.,Rodríguez-Sotres, Rogelio,Lira-Rocha, Alfonso

, p. 2976 - 2988 (2016/11/09)

Novel thiazolo[5,4-b]quinoline derivatives were prepared with or without a (2-(azacycloalkyl)ethyl)amino substituent at the 2-position. The effect of the substituent at 2-position on cytotoxic activity, DNA-intercalation and cytotoxic properties were evaluated. Substituents at 2-position bearing an aliphatic amine favored cytotoxicity, while removal of these substituents resulted in low or negligible cytotoxic properties. Additionally, the in silico predicted binding mode of the novel compounds into DNA correlated with the experimental intercalation data. These results suggest a strong influence of the substituent at 2-position on the DNA intercalation properties.

Synthesis of condensed pyrimidines in one-pot reaction from pyranoquinolines and BMMAs

Nahas, Nariman M.

, p. 51 - 54 (2008/09/19)

New pentacyclic heterocycles of the type 3a-e -5a-e were synthesized by one - pot reaction of the amino-cyano pyrano[3,2-h]quinolines la-e with BMMAs ( e.g. Ethyl N-[bis (methylsulfanyl) methylene] glycinate, ethyl 2[bis (methylsulfanyl) methylene]-1-methylhydrazine carboxylate and / or ethyl N[bis(methylsulfanyl) methylene]- ss-alaninate). All the synthesized derivatives were identified by conventional methods (IR, 1HNMR, MS) and elemental analysis. Antifungal tests were also performed.

Fused pyrimidines. Part II: Synthesis and antimicrobial activity of some furo[3,2-e]imidazo[1,2-c]pyrimidines and furo[2,3-d]pyrimidines

Bhuiyan,Rahman, Khandker M. M.,Hossain,Rahim,Hossain

, p. 633 - 636 (2007/10/03)

2-Amino-4,5-diphenylfuran-3-carbonitrile (2) reacted with N-[bis(methylthio)methylene]glycine ethyl ester (1) to afford a double cyclized product 5-methylthio-8,9-diphenylfuro[3,2-e]imidazo[1,2-c]pyrimidin-2(3H)-one (3). Compound 2 also reacts with benzon

Annelated pyrrolo-pyrimidines from amino-cyanopyrroles and BMMAs as leads for new DNA-interactive ring systems

Lauria, Antonino,Bruno, Marcella,Diana, Patrizia,Barraja, Paola,Montalbano, Alessandra,Cirrincione, Girolamo,Dattolo, Gaetano,Almerico, Anna Maria

, p. 1545 - 1553 (2007/10/03)

The efficient one-pot synthesis of several new tricyclic systems of type 1 and 2, obtained from the reaction of substituted 2-amino-3-cyanopyrroles and 3-amino-4-cyanopyrroles with BMMAs, is reported. The duration and yields of the reaction strongly depen

Triphosgene: A versatile reagent for the synthesis of azetidin-2-ones

Krishnaswamy,Govande,Gumaste,Bhawal,Deshmukh

, p. 2215 - 2225 (2007/10/03)

An efficient use of triphosgene, as an acid activator, for the synthesis of substituted azetidin-2-ones via ketene-imine cycloaddition reaction using various acids and imines have been described.

N-AMINO ESTERS (BMMA): NOVEL REAGENTS FOR ANNELATION OF PYRIMIDINE MOIETIES

Sauter, Fritz,Froehlich, Johannes,Blasl, Karin,Gewald, Karl

, p. 851 - 866 (2007/10/02)

New reagents for heterocyclic annelations containing a N-amino moiety (=BMMA) were developed and studied regarding their scope and limitations: one-pot reaction with (hetero)aromatic ortho-aminocarbonyl-type model compounds ("car

Synthesis of 4-Unsubstituted β-Lactams via Dithiocarbonimidates

Sharma, S. D.,Mehra, Usha,Khurana, J. P. S.,Pandhi, S. B.

, p. 990 - 992 (2007/10/02)

Cycloaddition of dithiocarbonimidate 1 to the ketene generated in situ from phenoxyacetylchloride in the presence of triethylamine affords the 4-dithioalkyl-2-azetidinones 2 in good yields.Facile conversion of 2 to the 4-unsubstituted β-lactams 3 can be accomplished by desulfurization with Raney-Nickel.Formation of several interesting products during attempts to bring a carbonyl function at C-4 in 2 has also been described.

A NOVEL SYNTHESIS OF THIAZOLES FROM DIMETHYL N-(ETHOXYCARBONYLMETHYL)IMINO DITHIOCARBONATE, CARBON DISULFIDE AND ALKYL HALIDES

Alvarez-Ibarra, C.,Davila, E.,Mateo, A.,Ortiz, P.,Quiroga, M. L.

, p. 6667 - 6670 (2007/10/02)

We report a new synthesis of thiazoles from a cyclocondensation reaction between dimethyl N-(ethoxycarbonylmethyl)iminodithiocarbonate (EMIC), carbon disulfide and alkylation of intermediate thiazole-2-thiolate with alkyl halides.

A NOVEL SYNTHESIS OF 2,3-DIHYDROOXAZOLES FROM DIMETHYL N-ETHOXYCARBONYLMETHYLIMINODITHIOCARBONATE AND AROMATIC ALDEHYDES

Ibarra, Alvarez C.,Cereceda, J. A.,Ortiz, P.,Vicente, A.,Quiroga, M. L.

, p. 243 - 246 (2007/10/02)

We report the synthesis of 5-aryl-2-ethoxycarbonyl-4-methylthio-2,3-dihydrooxazoles from a cyclocondensation reaction between dimethyl N-ethoxycarbonylmethyliminodithiocarbonate and aromatic aldehydes.

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