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1310367-49-7

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

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  • 1310367-49-7 Structure

  • Basic information

    1. Product Name: 3-amino-2-ethoxybenzoic acid
    2. Synonyms: 3-amino-2-ethoxybenzoic acid
    3. CAS NO:1310367-49-7
    4. Molecular Formula:
    5. Molecular Weight: 181.191
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1310367-49-7.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: 3-amino-2-ethoxybenzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-amino-2-ethoxybenzoic acid(1310367-49-7)
    11. EPA Substance Registry System: 3-amino-2-ethoxybenzoic acid(1310367-49-7)

  • 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: 1310367-49-7(Hazardous Substances Data)

1310367-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1310367-49-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,3,6 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1310367-49:
(9*1)+(8*3)+(7*1)+(6*0)+(5*3)+(4*6)+(3*7)+(2*4)+(1*9)=117
117 % 10 = 7
So 1310367-49-7 is a valid CAS Registry Number.

1310367-49-7Upstream product

1310367-49-7Downstream Products

1310367-49-7Relevant articles and documents

Highly selective one-pot synthesis of H-bonded pentagon-shaped circular aromatic pentamers

Qin, Bo,Ong, Wei Qiang,Ye, Ruijuan,Du, Zhiyun,Chen, Xiuying,Yan, Yan,Zhang, Kun,Su, Haibin,Zeng, Huaqiang

, p. 5419 - 5421 (2011)

One-pot, multi-molecular macrocyclization allows the highly selective preparation of pentagon-shaped circular aromatic pentamers mediated by an inward-pointing continuous hydrogen-bonding network.

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