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1070867-08-1

C71H87NO7 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1070867-08-1 Structure

  • Basic information

    1. Product Name: C71H87NO7
    2. Synonyms: C71H87NO7
    3. CAS NO:1070867-08-1
    4. Molecular Formula:
    5. Molecular Weight: 1066.47
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1070867-08-1.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: C71H87NO7(CAS DataBase Reference)
    10. NIST Chemistry Reference: C71H87NO7(1070867-08-1)
    11. EPA Substance Registry System: C71H87NO7(1070867-08-1)

  • 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: 1070867-08-1(Hazardous Substances Data)

1070867-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1070867-08-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,0,8,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1070867-08:
(9*1)+(8*0)+(7*7)+(6*0)+(5*8)+(4*6)+(3*7)+(2*0)+(1*8)=151
151 % 10 = 1
So 1070867-08-1 is a valid CAS Registry Number.

1070867-08-1Downstream Products

1070867-08-1Relevant articles and documents

Synthesis of new chiral calix[4]azacrowns for enantiomeric recognition of carboxylic acids

Demirtas, Havva Nur,Bozkurt, Selahattin,Durmaz, Mustafa,Yilmaz, Mustafa,Sirit, Abdulkadir

, p. 2020 - 2025 (2008)

Two novel chiral calix[4]azacrown ethers 4 and 5 bearing a furfuryl group on the nitrogen atom were developed by the reaction of dibromo- or ditosyl derivatives of p-tert-butylcalix[4]arenes 2 and 3 with a chiral diol, 1. The enantioselective recognition of these receptors towards the enantiomers of racemic carboxylic acids has been studied by 1H NMR spectroscopy. The molar ratio and the association constants of the chiral compounds 4 and 5 with each of the enantiomers of guest molecules were determined by using Job plots and a nonlinear least-squares fitting method, respectively. The Job plots indicate that both of the hosts form 1:1 instantaneous complexes with (R)- or (S)-mandelic acid and (l)- or (d)-dibenzoyltartaric acid. The receptors exhibited different chiral recognition abilities towards the enantiomers of racemic guests.

Chiral calix[4]azacrowns for enantiomeric recognition of amino acid derivatives

Demirtas, Havva Nur,Bozkurt, Selahattin,Durmaz, Mustafa,Yilmaz, Mustafa,Sirit, Abdulkadir

experimental part, p. 3014 - 3018 (2009/06/06)

In this study the synthesis of novel chiral calix[4]azacrown derivatives has been reported. The enantioselectivity of chiral receptors was investigated by using UV-vis spectroscopy. All the chiral calix[4]arene derivatives exhibited certain chiral recogni

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