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CAS

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425634-14-6

D-Glucitol, 2,5-anhydro-1,4-dideoxy-4-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 425634-14-6 Structure

  • Basic information

    1. Product Name: D-Glucitol, 2,5-anhydro-1,4-dideoxy-4-methyl- (9CI)
    2. Synonyms: D-Glucitol, 2,5-anhydro-1,4-dideoxy-4-methyl- (9CI)
    3. CAS NO:425634-14-6
    4. Molecular Formula: C7H14O3
    5. Molecular Weight: 146.18426
    6. EINECS: N/A
    7. Product Categories: ALCOHOL
    8. Mol File: 425634-14-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 270.3±15.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.080±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.38±0.70(Predicted)
    10. CAS DataBase Reference: D-Glucitol, 2,5-anhydro-1,4-dideoxy-4-methyl- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: D-Glucitol, 2,5-anhydro-1,4-dideoxy-4-methyl- (9CI)(425634-14-6)
    12. EPA Substance Registry System: D-Glucitol, 2,5-anhydro-1,4-dideoxy-4-methyl- (9CI)(425634-14-6)

  • 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: 425634-14-6(Hazardous Substances Data)

425634-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 425634-14-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,5,6,3 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 425634-14:
(8*4)+(7*2)+(6*5)+(5*6)+(4*3)+(3*4)+(2*1)+(1*4)=136
136 % 10 = 6
So 425634-14-6 is a valid CAS Registry Number.

425634-14-6Downstream Products

425634-14-6Relevant articles and documents

Stereoselective synthesis of tetrahydrofurans via formal [3+2]-cycloaddition of aldehydes and allylsilanes. Formal total synthesis of the muscarine alkaloids (-)-allomuscarine and (+)-epimuscarine

Angle, Steven R.,El-Said, Nahla A.

, p. 3608 - 3613 (2007/10/03)

The stereoselective synthesis of tetrahydrofurans was achieved by formal [3+2]-cycloaddition of allyl and crotylsilanes with α-triethylsilyloxy aldehydes. The scope of the reaction was examined by using different α-substituted aldehydes and different subs

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