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115127-03-2

N-cinnamoylamino glycine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115127-03-2 Structure

  • Basic information

    1. Product Name: N-cinnamoylamino glycine
    2. Synonyms: N-cinnamoylamino glycine
    3. CAS NO:115127-03-2
    4. Molecular Formula:
    5. Molecular Weight: 187.198
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115127-03-2.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: N-cinnamoylamino glycine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-cinnamoylamino glycine(115127-03-2)
    11. EPA Substance Registry System: N-cinnamoylamino glycine(115127-03-2)

  • 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: 115127-03-2(Hazardous Substances Data)

115127-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115127-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,2 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115127-03:
(8*1)+(7*1)+(6*5)+(5*1)+(4*2)+(3*7)+(2*0)+(1*3)=82
82 % 10 = 2
So 115127-03-2 is a valid CAS Registry Number.

115127-03-2Relevant articles and documents

One-pot synthesis of 2,4,5-trisubstituted oxazoles from N-acyl amino acids by a combination of cyclodehydration with N,N′-diisopropylcarbodiimide and Wittig olefination

Huang, Wenhua,Dong, Guangping,Mijiti, Zumureti

experimental part, p. 977 - 981 (2012/02/13)

By a combination of cyclodehydration of N-acyl amino acids with N,N′-diisopropylcarbodiimide (DIC) and non-classical Wittig olefination of the resultant 5(4H)-oxazolones with Ph3PCHCN and Ph 3PCHCOOEt, 5-oxazoleacetonitriles and 5-oxazoleacetates were synthesized in one-pot in 41-85% and 57-70% yields, respectively.

Synthesis of 4-Arylidene--1,2-disubstituted-Δ2-imidazolin-5-ones

Kumar, Pradeep,Mukerjee, Arya K.

, p. 416 - 418 (2007/10/02)

Addition of 2-substituted-5-oxo-4,5-dihydro-1,3-oxazoles (5-oxazolones) (3) to imines in benzene leads to the formation of 4-arylidene-Δ2-1,3-oxazolin-5-ones (8) which undergo aminolysis and subsequent cyclisation to the corresponding 4-arylidene-1,2-disubstituted-Δ2-imidazolin-5-ones (10) on heating under reflux in gl. acetic acid.

Reactions of 2-Substituted 5-Oxazolones with Imines Carrying a Vicinal Hydroxyl Group & Salicylaldehyde

Kumar, Pradeep,Mukerjee, Arya K.

, p. 704 - 707 (2007/10/02)

5-Oxazolones, generated by cyclising N-acylglycines with ethyl chloroformate, react with imines carrying a vicinal hydroxyl group and also with salicylaldehyde.Unsaturated 5-oxazolone or 3-N-acylaminocoumarin is obtained depending on the type of reactants.

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