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212912-11-3

1,3-di-[N-benzyl-N-[(isobutyloxy)carbonyl]amino]-2-hydroxypropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 212912-11-3 Structure

  • Basic information

    1. Product Name: 1,3-di-[N-benzyl-N-[(isobutyloxy)carbonyl]amino]-2-hydroxypropane
    2. Synonyms: 1,3-di-[N-benzyl-N-[(isobutyloxy)carbonyl]amino]-2-hydroxypropane
    3. CAS NO:212912-11-3
    4. Molecular Formula:
    5. Molecular Weight: 470.609
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 212912-11-3.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: 1,3-di-[N-benzyl-N-[(isobutyloxy)carbonyl]amino]-2-hydroxypropane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-di-[N-benzyl-N-[(isobutyloxy)carbonyl]amino]-2-hydroxypropane(212912-11-3)
    11. EPA Substance Registry System: 1,3-di-[N-benzyl-N-[(isobutyloxy)carbonyl]amino]-2-hydroxypropane(212912-11-3)

  • 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: 212912-11-3(Hazardous Substances Data)

212912-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 212912-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,9,1 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 212912-11:
(8*2)+(7*1)+(6*2)+(5*9)+(4*1)+(3*2)+(2*1)+(1*1)=93
93 % 10 = 3
So 212912-11-3 is a valid CAS Registry Number.

212912-11-3Relevant articles and documents

Synthesis and anti-HIV activities of symmetrical N1,N3-dibenzyl-2- hydroxy-propane derivatives

Medou,Bouygues,Rocheblave,Chermann,Kraus

, p. 1861 - 1866 (1998)

We report the synthesis and the anti-HIV activities of new C2- symmetrical and achiral N1,N3-dibenzyl-2-hydroxy-propane isosteres. Some of them showed significant inhibitory activity with respect to HIV-infected MT4 cells

Synthesis and anti-HIV activity of α-thiophenoxy-hydroxyethylamide derivatives

Medou, Martial,Priem, Ghislaine,Rocheblave, Luc,Pepe, Gerard,Meyer, Monique,Chermann, Jean-Claude,Kraus, Jean-Louis

, p. 625 - 638 (2007/10/03)

A series of new anti-HIV derivatives containing a novel α- thiophenoxyhydroxyethylamide core have been synthesized, using S- phenylbenzenethiosulfonate as the thiosulfenylating reagent. Some of the new synthesized compounds (1a, 1c, 1g, 1i, 1j and 1l) inhibited HIV replication in cell culture assays (syncytia formation) with effective concentrations (EC50) ranging from 0. 1-1 μM. Incorporation of thiophenoxy substitution within various pseudomimetic peptide backbones provided a series of highly potent HIV inhibitors.

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