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1-Phenyl-2-(isopropylamino)-1-propanol is an organic compound with the molecular formula C??H??N O. It is a colorless liquid at room temperature and is soluble in water. 1-phenyl-2-(isopropylamino)-1-propanol is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the development of new drugs and as a chiral auxiliary in asymmetric synthesis. Due to its unique structure, it has attracted significant attention in the field of organic chemistry and drug discovery.

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  • 4830-43-7 Structure
  • Basic information

    1. Product Name: 1-phenyl-2-(isopropylamino)-1-propanol
    2. Synonyms:
    3. CAS NO:4830-43-7
    4. Molecular Formula:
    5. Molecular Weight: 193.289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4830-43-7.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: 1-phenyl-2-(isopropylamino)-1-propanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenyl-2-(isopropylamino)-1-propanol(4830-43-7)
    11. EPA Substance Registry System: 1-phenyl-2-(isopropylamino)-1-propanol(4830-43-7)
  • 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: 4830-43-7(Hazardous Substances Data)

4830-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4830-43-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4830-43:
(6*4)+(5*8)+(4*3)+(3*0)+(2*4)+(1*3)=87
87 % 10 = 7
So 4830-43-7 is a valid CAS Registry Number.

4830-43-7Relevant articles and documents

Reductive Alkylation of β-Alkanolamines with Carbonyl Compounds and Sodium Borohydride

Saavedra, Joseph E.

, p. 2271 - 2273 (2007/10/02)

A synthesis of secondary alkylalkanolamines from primary alkanolamines in a rapid process in which overalkylation is virtually suppressed is described.The procedure combines the ease of formation of oxazolidines from alkanolamines with aldehydes or ketones in absolute ethanol and the lability of the newly formed C-O bond toward sodium borohydrode.The entire process is carried out in 15-35 min depending on the carbonyl substrate.

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