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120566-91-8

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  • 120566-91-8 Structure

  • Basic information

    1. Product Name: spinosine
    2. Synonyms: spinosine
    3. CAS NO:120566-91-8
    4. Molecular Formula: C19H21NO4
    5. Molecular Weight: 327.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 120566-91-8.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: spinosine(CAS DataBase Reference)
    10. NIST Chemistry Reference: spinosine(120566-91-8)
    11. EPA Substance Registry System: spinosine(120566-91-8)

  • 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: 120566-91-8(Hazardous Substances Data)

120566-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120566-91-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,5,6 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 120566-91:
(8*1)+(7*2)+(6*0)+(5*5)+(4*6)+(3*6)+(2*9)+(1*1)=108
108 % 10 = 8
So 120566-91-8 is a valid CAS Registry Number.

120566-91-8Downstream Products

120566-91-8Relevant articles and documents

HEXAHYDRODIBENZO[A,G]QUINOLIZINE COMPOUND, PREPARATION METHOD THEREOF, PHARMACEUTICAL COMPOSITION AND USE THEREOF

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Paragraph 0092; 0115, (2014/04/03)

The present invention relates to a novel hexahydrodibenzo[a,g]quinoline compound represented by general formula (I) and its derivatives, enantiomer, diastereoisomer, raceme and mixtures thereof, as well as pharmaceutically acceptable salts thereof. The pr

Studies on Mannich Reaction of 1-Benzyltetrahydroisoquinolines

Bhakuni, D. S.,Kumar, Praveen

, p. 417 - 421 (2007/10/02)

The effect of substituents in Mannich cyclisation reaction of 1-benzyltetrahydroisoquinolines has been studied.Both para- and ortho-cyclisation products are formed when hydroxyl groups are present in the benzene ring of the benzylic moiety whereas only pa

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