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2-aminoacetyl-3-nitrobenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1234834-07-1 Structure
  • Basic information

    1. Product Name: 2-aminoacetyl-3-nitrobenzoic acid
    2. Synonyms: 2-aminoacetyl-3-nitrobenzoic acid
    3. CAS NO:1234834-07-1
    4. Molecular Formula:
    5. Molecular Weight: 224.173
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1234834-07-1.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-aminoacetyl-3-nitrobenzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-aminoacetyl-3-nitrobenzoic acid(1234834-07-1)
    11. EPA Substance Registry System: 2-aminoacetyl-3-nitrobenzoic acid(1234834-07-1)
  • 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: 1234834-07-1(Hazardous Substances Data)

1234834-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1234834-07-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,4,8,3 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1234834-07:
(9*1)+(8*2)+(7*3)+(6*4)+(5*8)+(4*3)+(3*4)+(2*0)+(1*7)=141
141 % 10 = 1
So 1234834-07-1 is a valid CAS Registry Number.

1234834-07-1Upstream product

1234834-07-1Relevant articles and documents

Benzimidazole-4-Carboxamide Derivatives, Their Preparation Methods, Pharmaceutical Compositions And Their Uses

-

, (2011/11/12)

The present invention relates to the benzimidazole-4-carboxamide derivatives, their preparation methods, pharmaceutical compositions and their uses; wherein X represents monosubstituted or bissubstituted or polysubstitued C1-C14 alkoxy, monosubstituted or bisubstituted or polysubstitued C1-C14 alkyl, monosubstituted or bisubstituted or polysubstitued C2-C14 alkenyl, monosubstituted or bisubstituted or polysubstitued C6-C14 aryl, or monosubstituted or bisubstituted or polysubstitued 5 to 6 membered heterocyclic group, or monosubstituted or bisubstituted or polysubstitued fused ring group containing nitrogen heteroatom; Y represents hydrogen, monosubstituted or bisubstituted or polysubstitued C1-C16 alkyl, monosubstituted or bisubstituted or polysubstitued C6-C12 aryl, or monosubstituted or bisubstituted or polysubstitued 5 to 6 membered heterocyclic group, or monosubstituted or bisubstituted or polysubstitued fused ring group containing nitrogen heteroatom. The derivatives of the present invention have the functions of antiviral medicine.

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