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Cyclohexanecarbonitrile, 1-hydroxy-4-(1-methylethyl)-, trans- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Cyclohexanecarbonitrile, 1-hydroxy-4-(1-methylethyl)-, trans- (9CI)

    Cas No: 251324-79-5

  • USD $ 1.9-2.9 / Gram

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  • 251324-79-5 Structure
  • Basic information

    1. Product Name: Cyclohexanecarbonitrile, 1-hydroxy-4-(1-methylethyl)-, trans- (9CI)
    2. Synonyms: Cyclohexanecarbonitrile, 1-hydroxy-4-(1-methylethyl)-, trans- (9CI)
    3. CAS NO:251324-79-5
    4. Molecular Formula: C10H17NO
    5. Molecular Weight: 167.24808
    6. EINECS: N/A
    7. Product Categories: ISOPROPYL
    8. Mol File: 251324-79-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cyclohexanecarbonitrile, 1-hydroxy-4-(1-methylethyl)-, trans- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanecarbonitrile, 1-hydroxy-4-(1-methylethyl)-, trans- (9CI)(251324-79-5)
    11. EPA Substance Registry System: Cyclohexanecarbonitrile, 1-hydroxy-4-(1-methylethyl)-, trans- (9CI)(251324-79-5)
  • 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: 251324-79-5(Hazardous Substances Data)

251324-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 251324-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,3,2 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 251324-79:
(8*2)+(7*5)+(6*1)+(5*3)+(4*2)+(3*4)+(2*7)+(1*9)=115
115 % 10 = 5
So 251324-79-5 is a valid CAS Registry Number.

251324-79-5Downstream Products

251324-79-5Relevant articles and documents

Stereoselective synthesis of cis-p-menth-8-ene-1,7-diol, cis-p-menthane-1,7-diol, and cis-p-menthane-1,7,8-triol

Kobler, Christoph,Effenberger, Franz

, p. 2783 - 2787 (2007/10/03)

The natural products cis-p-mentharie-1,7-diol (cis-IV), cis-p-menth-8-ene-1,7-diol (cis-I) and cis-p-menthane-1,7,8-triol (cis-II) are obtained starting from the corresponding cis-cyanohydrins, cis-2 and cis-7, respectively, by chemical transformation of

Hydroxynitrile lyase-catalyzed addition of HCN to 4-substituted cyclohexanones: Stereoselective preparation of tetronic acids

Effenberger, Franz,Roos, Juergen,Kobler, Christoph,Buehler, Holger

, p. 671 - 679 (2007/10/03)

The addition of HCN to 4-alkylcyclohexanones 1 to give cyanohydrins 2 is strongly catalyzed by hydroxynitrile lyases (HNLs). With PaHNL, from bitter almond, trans-addition occurs almost exclusively, yielding trans-2. With MeHNL, from cassava, cis-addition

cis-trans selectivity of enzyme-catalyzed additions to 4-substituted cyclohexanones - Correlation with the Prelog/Ringold model of enzymatic hydrogenation

Effenberger, Franz,Roos, Juergen,Kobler, Christoph

, p. 1876 - 1879 (2007/10/03)

The choice of enzyme is decisive: for the enzyme-catalyzed addition of HCN to 4-substituted cyclohexanones 1, highly selective biocatalysts are available that allow control to yield the cis or the trans addition product 2. Modeling of the S enzyme - subst

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