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CAS

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1081979-44-3

methyl 4-{[2-(hydroxymethyl)acryloyl](methyl)amino}benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1081979-44-3 Structure

  • Basic information

    1. Product Name: methyl 4-{[2-(hydroxymethyl)acryloyl](methyl)amino}benzoate
    2. Synonyms: methyl 4-{[2-(hydroxymethyl)acryloyl](methyl)amino}benzoate
    3. CAS NO:1081979-44-3
    4. Molecular Formula:
    5. Molecular Weight: 249.266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1081979-44-3.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: methyl 4-{[2-(hydroxymethyl)acryloyl](methyl)amino}benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4-{[2-(hydroxymethyl)acryloyl](methyl)amino}benzoate(1081979-44-3)
    11. EPA Substance Registry System: methyl 4-{[2-(hydroxymethyl)acryloyl](methyl)amino}benzoate(1081979-44-3)

  • 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: 1081979-44-3(Hazardous Substances Data)

1081979-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1081979-44-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,1,9,7 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1081979-44:
(9*1)+(8*0)+(7*8)+(6*1)+(5*9)+(4*7)+(3*9)+(2*4)+(1*4)=183
183 % 10 = 3
So 1081979-44-3 is a valid CAS Registry Number.

1081979-44-3Relevant articles and documents

Metal-free oxidative spirocyclization of hydroxymethylacrylamide with 1,3-dicarbonyl compounds: A new route to spirooxindoles

Wang, Hua,Guo, Li-Na,Duan, Xin-Hua

, p. 5254 - 5257 (2013/11/06)

A metal-free oxidative spirocyclization of hydroxymethylacrylamide with 1,3-dicarbonyl compounds is described. The reaction proceeds through tandem dual C-H functionalization and intramolecular dehydration, in which two new C-C bonds and one C-O bond were formed. This method affords a novel and straightforward access to various spirooxindoles under mild conditions.

Photochemical elimination of leaving groups from zwitterionic intermediates generated via electrocyclic ring closure of α,β-unsaturated anilides

Jia, Jinli,Sarker, Majher,Steinmetz, Mark G.,Shukla, Ruchi,Rathore, Rajendra

experimental part, p. 8867 - 8879 (2009/04/04)

(Chemical Equation Presented) Methacrylanilides, ArN(CH3) COC(CH2LG)=CH2, with allylic leaving groups (LG - = BocAla, PhCO2-, PhCH2CO 2-, PhO-) u

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