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1142908-01-7

C7H6N2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1142908-01-7 Structure

  • Basic information

    1. Product Name: C7H6N2O
    2. Synonyms:
    3. CAS NO:1142908-01-7
    4. Molecular Formula:
    5. Molecular Weight: 134.137
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1142908-01-7.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: C7H6N2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C7H6N2O(1142908-01-7)
    11. EPA Substance Registry System: C7H6N2O(1142908-01-7)

  • 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: 1142908-01-7(Hazardous Substances Data)

1142908-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1142908-01-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,2,9,0 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1142908-01:
(9*1)+(8*1)+(7*4)+(6*2)+(5*9)+(4*0)+(3*8)+(2*0)+(1*1)=127
127 % 10 = 7
So 1142908-01-7 is a valid CAS Registry Number.

1142908-01-7Downstream Products

1142908-01-7Relevant articles and documents

Enzymatic kinetic resolution of racemic cyanohydrins via enantioselective acylation

Xu, Qing,Xie, Yongli,Geng, Xiaohong,Chen, Peiran

, p. 624 - 630 (2010)

Enzymatic kinetic resolution of a series of aromatic and aliphatic cyanohydrins in organic media has been investigated. The behavior of potential lipases, molecular sieves, acyl reagent, reaction temperature, and organic solvents on the kinetic resolution was studied. The influence of substrate structure, steric, and electronic nature and position of the aryl substituent on the enantioselectivity was discussed. Under the optimized reaction conditions, good enantioselectivity could be achieved for most of the investigated compounds. Specifically, substrates 1a, 1c, 1d, 1f, 1u could be resolved with the kinetic enantiomer ratio (E) higher than 200.

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