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3-((3-aminopropyl)amino)phenol hydrobromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1394078-18-2 Structure
  • Basic information

    1. Product Name: 3-((3-aminopropyl)amino)phenol hydrobromide
    2. Synonyms: 3-((3-aminopropyl)amino)phenol hydrobromide
    3. CAS NO:1394078-18-2
    4. Molecular Formula:
    5. Molecular Weight: 247.135
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1394078-18-2.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: 3-((3-aminopropyl)amino)phenol hydrobromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-((3-aminopropyl)amino)phenol hydrobromide(1394078-18-2)
    11. EPA Substance Registry System: 3-((3-aminopropyl)amino)phenol hydrobromide(1394078-18-2)
  • 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: 1394078-18-2(Hazardous Substances Data)

1394078-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1394078-18-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,0,7 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1394078-18:
(9*1)+(8*3)+(7*9)+(6*4)+(5*0)+(4*7)+(3*8)+(2*1)+(1*8)=182
182 % 10 = 2
So 1394078-18-2 is a valid CAS Registry Number.

1394078-18-2Downstream Products

1394078-18-2Relevant articles and documents

Bifunctionalised long-wavelength fluorescent probes for biological applications

Firmino, A. Daniela G.,Gon?alves, M. Sameiro T.

, p. 4946 - 4950 (2012)

The synthesis of benzo[a]phenoxazinium chlorides which are bifunctionalised in position 2 with 4-ethoxy-4-oxobutoxyl, 3-hydroxypropoxyl or 3-chloropropoxyl groups, and in position 9 with the (aminopropyl)amino group, was efficiently performed. The covalent labelling of valine was carried out by using one of the new fluorophores obtained. Photophysical studies in the homogeneous media of ethanol, distilled water and simulated physiological conditions revealed that all the compounds absorbed and emitted from 610 to 651 nm.

BENZOPHENOXAZINE DERIVATIVES FOR DIAGNOSIS OF NEOPLASIA OR INFECTION

-

Paragraph 0067, (2019/10/29)

The present disclosure is related to the synthesis and applications of a benzo[a]phenoxazine. It displays good photophysical properties, such as high molar extinction coefficient, good fluorescence quantum yield and solubility in water. The present invent

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