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126354-22-1

2'-methyl-5'-cyano-3β-hydroxyandrost-5-eno<17,16-c>pyridine-2(1H)-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126354-22-1 Structure

  • Basic information

    1. Product Name: 2'-methyl-5'-cyano-3β-hydroxyandrost-5-eno<17,16-c>pyridine-2(1H)-thione
    2. Synonyms: 2'-methyl-5'-cyano-3β-hydroxyandrost-5-eno<17,16-c>pyridine-2(1H)-thione
    3. CAS NO:126354-22-1
    4. Molecular Formula:
    5. Molecular Weight: 394.581
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126354-22-1.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: 2'-methyl-5'-cyano-3β-hydroxyandrost-5-eno<17,16-c>pyridine-2(1H)-thione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2'-methyl-5'-cyano-3β-hydroxyandrost-5-eno<17,16-c>pyridine-2(1H)-thione(126354-22-1)
    11. EPA Substance Registry System: 2'-methyl-5'-cyano-3β-hydroxyandrost-5-eno<17,16-c>pyridine-2(1H)-thione(126354-22-1)

  • 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: 126354-22-1(Hazardous Substances Data)

126354-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126354-22-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,5 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126354-22:
(8*1)+(7*2)+(6*6)+(5*3)+(4*5)+(3*4)+(2*2)+(1*2)=111
111 % 10 = 1
So 126354-22-1 is a valid CAS Registry Number.

126354-22-1Relevant articles and documents

CYCLIZATION OF NITRILES. XXVII. SYNTHESIS OF ANNELLATED PYRIDINES AND THIENOPYRIDINES BASED ON PREGNA-5,16-DIEN-3β-OL-20-ONE AND METHYLENE-ACTIVE NITRILES. MOLECULAR AND CRYSTAL STRUCTURE OF 3'-AMINO-6'-METHYL-2'-CYANO-3Β-HYDROXYANDROST-5-ENOTHIENOPYRIDINE

Klokol, G. V.,Sharanin, Yu. A.,Promonenkov, V. K.,Litvinov, V. P.,Bogdanov, V. S.,et al.

, p. 1616 - 1625 (2007/10/02)

The addition of methylene-active nitriles to pregna-5,16-dien-3β-ol-20-one acetate by Michael rection takes place stereoselectively and leads t the formation of 16α-substituted pregna-5-en-3β-ol-20-ones. (5-Pregnen-3β-ol-20-on-16α-yl)cyanothioacetamide was converted into 16α-(4-aryl-2-thiazolyl)pregna-5-en-3β-ol-20-ones and 2'-methyl-5'-cyano-3β-hydroxyandrost-5-enopyridine-6'(1'H)-thione.Alkylation of the latter gave 2'-substituted 3'-amino-6'-methyl-3β-hydroxyandrost-5-enothienopyridines.The crystals of3'-amino-6'-methyl-2'-cyano-3β-hydroxyandrost-5-enothienopyridine are constructed of two symmetrically independent molecules.

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