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CAS

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164203-06-9

(S)-1-nitro-2-propanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 164203-06-9 Structure

  • Basic information

    1. Product Name: (S)-1-nitro-2-propanol
    2. Synonyms:
    3. CAS NO:164203-06-9
    4. Molecular Formula:
    5. Molecular Weight: 105.093
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 164203-06-9.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: (S)-1-nitro-2-propanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-nitro-2-propanol(164203-06-9)
    11. EPA Substance Registry System: (S)-1-nitro-2-propanol(164203-06-9)

  • 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: 164203-06-9(Hazardous Substances Data)

164203-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164203-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,2,0 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 164203-06:
(8*1)+(7*6)+(6*4)+(5*2)+(4*0)+(3*3)+(2*0)+(1*6)=99
99 % 10 = 9
So 164203-06-9 is a valid CAS Registry Number.

164203-06-9Downstream Products

164203-06-9Relevant articles and documents

Highly enantioselective asymmetric Henry reaction catalyzed by novel chiral phase transfer catalysts derived from cinchona alkaloids

Vijaya, Ponmuthu Kottala,Murugesan, Sepperumal,Siva, Ayyanar

supporting information, p. 10101 - 10109 (2016/11/06)

A new type of di-site chiral phase transfer catalyst has been designed and synthesized from cinchona alkaloids as a chiral precursor. The prepared catalysts are applied in the asymmetric Henry reaction to a wide range of aldehydes using mild concentration

Lipase catalysed resolution of nitro aldol adducts

Sorgedrager, Menno J.,Malpique, Rita,Van Rantwijk, Fred,Sheldon, Roger A.

, p. 1295 - 1299 (2007/10/03)

The kinetic resolution of a range of 1-nitro-2-alkanols by lipase-catalysed esterification using various lipases and succinic anhydride as an acyl donor has been studied. E values of up to 100 were obtained with Novozym 435 in the resolution of 1-nitro-2-pentanol with succinic anhydride in TBME. Acylation with succinic anhydride proved much more enantioselective than with vinyl acetate.

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