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CAS

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138611-11-7

(2R,3R)-3-tert-Butylamino-3-phenyl-propane-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138611-11-7 Structure

  • Basic information

    1. Product Name: (2R,3R)-3-tert-Butylamino-3-phenyl-propane-1,2-diol
    2. Synonyms:
    3. CAS NO:138611-11-7
    4. Molecular Formula:
    5. Molecular Weight: 223.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138611-11-7.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: (2R,3R)-3-tert-Butylamino-3-phenyl-propane-1,2-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R)-3-tert-Butylamino-3-phenyl-propane-1,2-diol(138611-11-7)
    11. EPA Substance Registry System: (2R,3R)-3-tert-Butylamino-3-phenyl-propane-1,2-diol(138611-11-7)

  • 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: 138611-11-7(Hazardous Substances Data)

138611-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138611-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,1 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138611-11:
(8*1)+(7*3)+(6*8)+(5*6)+(4*1)+(3*1)+(2*1)+(1*1)=117
117 % 10 = 7
So 138611-11-7 is a valid CAS Registry Number.

138611-11-7Downstream Products

138611-11-7Relevant articles and documents

Regioselective ring opening of chiral epoxyalcohols by primary amines

Canas, Marc,Poch, Marta,Verdaguer, Xavier,Moyano, Albert,Pericas, Miquel A.,Riera, Antoni

, p. 6931 - 6934 (1991)

A reinvestigation of the titanium(IV)-mediated reaction of primary amines with chiral 2,3-epoxyalcohols shows that, contrary to previous reports, this reaction constitutes a general and practical process for the enantioselective synthesis of 3-amino-1,2-diols.

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