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CAS

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1095268-94-2

4-[(1R,2R)-2-(benzyloxy)cyclopentyl]-2,2-dimethyl-1,3-dioxolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1095268-94-2 Structure

  • Basic information

    1. Product Name: 4-[(1R,2R)-2-(benzyloxy)cyclopentyl]-2,2-dimethyl-1,3-dioxolane
    2. Synonyms: 4-[(1R,2R)-2-(benzyloxy)cyclopentyl]-2,2-dimethyl-1,3-dioxolane
    3. CAS NO:1095268-94-2
    4. Molecular Formula:
    5. Molecular Weight: 276.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1095268-94-2.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: 4-[(1R,2R)-2-(benzyloxy)cyclopentyl]-2,2-dimethyl-1,3-dioxolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[(1R,2R)-2-(benzyloxy)cyclopentyl]-2,2-dimethyl-1,3-dioxolane(1095268-94-2)
    11. EPA Substance Registry System: 4-[(1R,2R)-2-(benzyloxy)cyclopentyl]-2,2-dimethyl-1,3-dioxolane(1095268-94-2)

  • 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: 1095268-94-2(Hazardous Substances Data)

1095268-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1095268-94-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,5,2,6 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1095268-94:
(9*1)+(8*0)+(7*9)+(6*5)+(5*2)+(4*6)+(3*8)+(2*9)+(1*4)=182
182 % 10 = 2
So 1095268-94-2 is a valid CAS Registry Number.

1095268-94-2Upstream product

1095268-94-2Relevant articles and documents

Synthesis of L- and D-4,6-dideoxyhexoses and 4,6-dideoxy-C-phenylglycosides from enzyme-generated products

Acetti, Daniela,Brenna, Elisabetta,Fuganti, Claudio,Gatti, Francesco G.,Malpezzi, Luciana,Serra, Stefano

, p. 5125 - 5134 (2008)

Optically active 1,3-diols 1 were prepared by biocatalysed routes. The synthetic versatility of compounds 1 as chiral building blocks was shown. The oxidative cleavage of the double bond afforded a carbonyl moiety, which allowed for elongation by Grignard addition and further derivatisation to make deoxy sugars readily available. The epoxidation of the same double bond allowed the direct intramolecular opening of the epoxide ring to generate deoxy C-phenylglycosides. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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