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123172-76-9

2-hydroxy-3-tert-butyl-α<1-(tertbutyloxycarbonylamino)-2-pyrrolidinyl>benzenemethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123172-76-9 Structure

  • Basic information

    1. Product Name: 2-hydroxy-3-tert-butyl-α<1-(tertbutyloxycarbonylamino)-2-pyrrolidinyl>benzenemethanol
    2. Synonyms: 2-hydroxy-3-tert-butyl-α<1-(tertbutyloxycarbonylamino)-2-pyrrolidinyl>benzenemethanol
    3. CAS NO:123172-76-9
    4. Molecular Formula:
    5. Molecular Weight: 349.47
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123172-76-9.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-hydroxy-3-tert-butyl-α<1-(tertbutyloxycarbonylamino)-2-pyrrolidinyl>benzenemethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-hydroxy-3-tert-butyl-α<1-(tertbutyloxycarbonylamino)-2-pyrrolidinyl>benzenemethanol(123172-76-9)
    11. EPA Substance Registry System: 2-hydroxy-3-tert-butyl-α<1-(tertbutyloxycarbonylamino)-2-pyrrolidinyl>benzenemethanol(123172-76-9)

  • 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: 123172-76-9(Hazardous Substances Data)

123172-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123172-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,1,7 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123172-76:
(8*1)+(7*2)+(6*3)+(5*1)+(4*7)+(3*2)+(2*7)+(1*6)=99
99 % 10 = 9
So 123172-76-9 is a valid CAS Registry Number.

123172-76-9Downstream Products

123172-76-9Relevant articles and documents

SYNTHESIS OF OPTICALLY-ACTIVE EPHEDRINE-LIKE COMPOUNDS via COORDINATED DIASTEREOSELECTIVE FRIEDEL-CRAFTS ALKYLATION OF PHENOL SYSTEMS

Bigi, Franca,Casnati, Giuseppe,Sartori, Giovanni,Araldi, Gianluca

, p. 413 - 419 (2007/10/02)

The first direct diastereoselective synthesis of ephedrine-like compounds has been performed by hydroxyalkylation of metal phenolates with N-protected α-amino aldehydes: β-amino-ortho-hydroxybenzyl alcohols were obtained with good to excellent diastereose

HIGHLY REGIO- AND DIASTEREOSELECTIVE FRIEDEL-CRAFTS ALKYLATION OF PHENOLS WITH α-AMINO ALDEHYDES. SYNTHESIS OF OPTICALLY ACTIVE EPHEDRINE-LIKE COMPOUNDS

Bigi, Franca,Casnati, Giuseppe,Sartori, Giovanni,Araldi, Gianluca,Bocelli, Gabriele

, p. 1121 - 1124 (2007/10/02)

The first direct diastereoselective synthesis of ephedrine-like compounds has been achieved by alkylation of metal phenolates with N-tert-butoxycarbonyl-α-amino aldehydes; β-amino-ortho-hydroxybenzyl alcohols were obtained with good to excellent diastereoselection.

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