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(2R,1'R)-2-<(1'-phenylpropyl)amino>-2-phenylethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131214-09-0 Structure
  • Basic information

    1. Product Name: (2R,1'R)-2-<(1'-phenylpropyl)amino>-2-phenylethanol
    2. Synonyms: (2R,1'R)-2-<(1'-phenylpropyl)amino>-2-phenylethanol
    3. CAS NO:131214-09-0
    4. Molecular Formula:
    5. Molecular Weight: 255.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131214-09-0.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: (2R,1'R)-2-<(1'-phenylpropyl)amino>-2-phenylethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,1'R)-2-<(1'-phenylpropyl)amino>-2-phenylethanol(131214-09-0)
    11. EPA Substance Registry System: (2R,1'R)-2-<(1'-phenylpropyl)amino>-2-phenylethanol(131214-09-0)
  • 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: 131214-09-0(Hazardous Substances Data)

131214-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131214-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,1 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 131214-09:
(8*1)+(7*3)+(6*1)+(5*2)+(4*1)+(3*4)+(2*0)+(1*9)=70
70 % 10 = 0
So 131214-09-0 is a valid CAS Registry Number.

131214-09-0Relevant articles and documents

Asymmetric synthesis of allyl- and α-allenylamines from chiral imines and alkynes via (η2-imine)Ti(O-i-Pr)2 complexes

Fukuhara, Kohki,Okamoto, Sentaro,Sato, Fumie

, p. 2145 - 2148 (2007/10/03)

(Matrix presented) The reaction of a divalent titanium reagent Ti(O-i-Pr)4/2i-PrMgX with optically active arylaldimines derived from arylaldehydes and O-methylphenylglycinol provided, in a highly diastereoselective manner, chiral (η2-imine)Ti(O-i-Pr) 2 complexes, which in turn reacted with 1-alkynes or propargyl compounds to give optically active allyl- and α-allenylamines, respectively.

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