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CAS

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58706-05-1

1,2:4,5-di-O-isopropylidene-3-O-methyl-D-chiro-inositol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 58706-05-1 Structure

  • Basic information

    1. Product Name: 1,2:4,5-di-O-isopropylidene-3-O-methyl-D-chiro-inositol
    2. Synonyms:
    3. CAS NO:58706-05-1
    4. Molecular Formula:
    5. Molecular Weight: 274.314
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 58706-05-1.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: 1,2:4,5-di-O-isopropylidene-3-O-methyl-D-chiro-inositol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2:4,5-di-O-isopropylidene-3-O-methyl-D-chiro-inositol(58706-05-1)
    11. EPA Substance Registry System: 1,2:4,5-di-O-isopropylidene-3-O-methyl-D-chiro-inositol(58706-05-1)

  • 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: 58706-05-1(Hazardous Substances Data)

58706-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58706-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,0 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58706-05:
(7*5)+(6*8)+(5*7)+(4*0)+(3*6)+(2*0)+(1*5)=141
141 % 10 = 1
So 58706-05-1 is a valid CAS Registry Number.

58706-05-1Downstream Products

58706-05-1Relevant articles and documents

Efficient synthetic routes to fluorinated isosteres of inositol and their effects on cellular growth

Kozikowski, Alan P.,Fauq, Abdul H.,Powis, Garth,Melder, Deborah C.

, p. 4528 - 4531 (2007/10/02)

Efficient synthetic routes to several fluorinated isosteres of inositol have been developed that are based upon the unexpected selectivity observed in the (diethylamido)sulfur trifluoride reaction of polyhydroxylated cyclohexane derivatives. The conversio

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