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251372-30-2

2-amino-3-(3-nitro-phenyl)-propionic acid 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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  • 251372-30-2 Structure

  • Basic information

    1. Product Name: 2-amino-3-(3-nitro-phenyl)-propionic acid ethyl ester
    2. Synonyms: 2-amino-3-(3-nitro-phenyl)-propionic acid ethyl ester
    3. CAS NO:251372-30-2
    4. Molecular Formula:
    5. Molecular Weight: 238.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 251372-30-2.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-amino-3-(3-nitro-phenyl)-propionic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-amino-3-(3-nitro-phenyl)-propionic acid ethyl ester(251372-30-2)
    11. EPA Substance Registry System: 2-amino-3-(3-nitro-phenyl)-propionic acid ethyl ester(251372-30-2)

  • 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: 251372-30-2(Hazardous Substances Data)

251372-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 251372-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,3,7 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 251372-30:
(8*2)+(7*5)+(6*1)+(5*3)+(4*7)+(3*2)+(2*3)+(1*0)=112
112 % 10 = 2
So 251372-30-2 is a valid CAS Registry Number.

251372-30-2Upstream product

251372-30-2Relevant articles and documents

Synthesis of Functionalised Phenylalanines Using Rhodium Catalysis in Water

Chapman, Christopher J.,Frost, Christopher G.

, p. 353 - 355 (2003)

The efficient synthesis of substituted phenylalanine-type amino acids using a rhodium-catalysed, conjugate addition of arylboronic acids is described. The reactions are run in water and use a low loading (0.5 mol %) of rhodium catalyst.

Use of 2-aminothiazoline derivatives as inhibitors of inducible no-synthase

-

, (2008/06/13)

The present invention relates to the use of 2-aminothiazoline derivatives of formula: in which either R1 is a hydrogen atom or an alkyl radical and R2 is an alkyl, -alk-NH2, —CH2—R3, —CH2—S

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