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1126489-60-8

benzyl N-((benzyloxy)carbonyl)-O-(5-(4-(1-butylpentyl)pyridinium-1-yl)pentanoyl)-L-threoninate bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1126489-60-8 Structure

  • Basic information

    1. Product Name: benzyl N-((benzyloxy)carbonyl)-O-(5-(4-(1-butylpentyl)pyridinium-1-yl)pentanoyl)-L-threoninate bromide
    2. Synonyms:
    3. CAS NO:1126489-60-8
    4. Molecular Formula:
    5. Molecular Weight: 711.737
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1126489-60-8.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: benzyl N-((benzyloxy)carbonyl)-O-(5-(4-(1-butylpentyl)pyridinium-1-yl)pentanoyl)-L-threoninate bromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl N-((benzyloxy)carbonyl)-O-(5-(4-(1-butylpentyl)pyridinium-1-yl)pentanoyl)-L-threoninate bromide(1126489-60-8)
    11. EPA Substance Registry System: benzyl N-((benzyloxy)carbonyl)-O-(5-(4-(1-butylpentyl)pyridinium-1-yl)pentanoyl)-L-threoninate bromide(1126489-60-8)

  • 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: 1126489-60-8(Hazardous Substances Data)

1126489-60-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1126489-60-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,6,4,8 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1126489-60:
(9*1)+(8*1)+(7*2)+(6*6)+(5*4)+(4*8)+(3*9)+(2*6)+(1*0)=158
158 % 10 = 8
So 1126489-60-8 is a valid CAS Registry Number.

1126489-60-8Downstream Products

1126489-60-8Relevant articles and documents

Hydroxy-α-amino acids modified by ionic liquid moieties: recoverable organocatalysts for asymmetric aldol reactions in the presence of water

Siyutkin, Dmitriy E.,Kucherenko, Alexander S.,Zlotin, Sergei G.

, p. 1366 - 1372 (2009)

New chiral ionic liquids bearing proline, serine or threonine moieties were synthesized. Compounds that contain 1-dodecylimidazolium or 4-(5-n-nonyl)-pyridinium cations and NTf2 or PF6 anions efficiently catalyze the asymmetric aldol reaction between aldehydes and ketones in the presence of water to generate aldols with high distereo- (up to 98:2) and enantioselectivity (up to >99% ee). 4-Hydroxyproline modified by the 4-(5-n-nonyl)-pyridinium hexafluorophosphate moiety retains its activity and selectivity over at least eight reaction cycles.

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