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151909-83-0

2,3,4-tri-O-methyl-6-O-trityl-D-glucitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151909-83-0 Structure

  • Basic information

    1. Product Name: 2,3,4-tri-O-methyl-6-O-trityl-D-glucitol
    2. Synonyms: 2,3,4-tri-O-methyl-6-O-trityl-D-glucitol
    3. CAS NO:151909-83-0
    4. Molecular Formula:
    5. Molecular Weight: 466.574
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151909-83-0.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: 2,3,4-tri-O-methyl-6-O-trityl-D-glucitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4-tri-O-methyl-6-O-trityl-D-glucitol(151909-83-0)
    11. EPA Substance Registry System: 2,3,4-tri-O-methyl-6-O-trityl-D-glucitol(151909-83-0)

  • 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: 151909-83-0(Hazardous Substances Data)

151909-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151909-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,9,0 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 151909-83:
(8*1)+(7*5)+(6*1)+(5*9)+(4*0)+(3*9)+(2*8)+(1*3)=140
140 % 10 = 0
So 151909-83-0 is a valid CAS Registry Number.

151909-83-0Relevant articles and documents

Asymmetric synthesis using reactions with modest group selectivity

Ward, Dale E.,Liu, YaDong,Rhee, Chung K.

, p. 1429 - 1446 (2007/10/02)

The isomeric purity of products from certain group-selective reactions can be significantly amplified when reactions can occur sequentially.The theoretical basis for a strategy that exploits reactions with modest enantiotopic group selectivity for asymmet

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