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2-Propanone, 1-(1-methyl-2-imidazolidinylidene)-, (1E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101998-53-2 Structure
  • Basic information

    1. Product Name: 2-Propanone, 1-(1-methyl-2-imidazolidinylidene)-, (1E)-
    2. Synonyms:
    3. CAS NO:101998-53-2
    4. Molecular Formula: C7H12N2O
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101998-53-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Propanone, 1-(1-methyl-2-imidazolidinylidene)-, (1E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propanone, 1-(1-methyl-2-imidazolidinylidene)-, (1E)-(101998-53-2)
    11. EPA Substance Registry System: 2-Propanone, 1-(1-methyl-2-imidazolidinylidene)-, (1E)-(101998-53-2)
  • 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: 101998-53-2(Hazardous Substances Data)

101998-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101998-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,9 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 101998-53:
(8*1)+(7*0)+(6*1)+(5*9)+(4*9)+(3*8)+(2*5)+(1*3)=132
132 % 10 = 2
So 101998-53-2 is a valid CAS Registry Number.

101998-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-methylimidazolidin-2-ylidene)propan-2-one

1.2 Other means of identification

Product number -
Other names (E)-2-(Acetylmethylene)-1-methylimidazolidine

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:101998-53-2 SDS

101998-53-2Downstream Products

101998-53-2Relevant articles and documents

Synthesis of Acetyl-Substituted Heterocyclic Ketene Aminals and Their Deactylation Reaction

Wang, He-Ting,Wang, Xiao-Jun,Huang, Zhi-Tang

, p. 2141 - 2145 (2007/10/02)

The acetyl-substituted heterocyclic ketene aminals 3-6 were synthesized by the reaction of ketene dithioacetals 2 with diamines.The deacetylation of heterocyclic diacetyl ketene-aminals by alkali was studied, and the corresponding monoacetyl derivatives were studied.

Synthesis of Ketene Aminals with an Imidazoline Ring by Condensation of 4,5-Dihydro-2-(methylthio)-1H-imidazoles with Active Methylene Compounds and Some Addition and Cyclocondensation Reactions

Huang, Zhi-tang,Tzai, Lu-hang

, p. 2208 - 2219 (2007/10/02)

The 4,5-dihydro-2-(methylthio)-1H-imidazoles 1a, b react with active methylene compounds 2a - f to afford the corresponding substituted methyleneimidazolines 3a - f and 4c - f by elimination of methanethiol.The reaction of compounds 2g - j, which contain a more active carbonyl group, with 1a gives 3g - i by elimination of a methylthio group as well as an acyl group, too. 3a, g - i react with esters of α,β-unsaturated acids to afford the corresponding imidazopyridines 5, 6, and 7 in an addition and cyclocondensation reaction sequence, but with diethyl azodicarboxylate only to give the addition product 8.

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