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102719-12-0

.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate is a complex chemical compound derived from D-arabino-Hexopyranose, featuring a hexopyranose ring, an anhydro-3-deoxy-4-O group, and an acetate functional group. This synthetic derivative also contains a phenylmethyl moiety, which, along with the acetate group, may alter its chemical properties and potential applications. .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate's structure suggests it could have relevance in carbohydrate chemistry and related fields, although further research is needed to fully understand its uses and properties.

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  • .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate

    Cas No: 102719-12-0

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  • 102719-12-0 Structure

  • Basic information

    1. Product Name: .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate
    2. Synonyms: .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate
    3. CAS NO:102719-12-0
    4. Molecular Formula: C15H18O5
    5. Molecular Weight: 278.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102719-12-0.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: .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate(102719-12-0)
    11. EPA Substance Registry System: .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate(102719-12-0)

  • 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: 102719-12-0(Hazardous Substances Data)

102719-12-0 Usage

Uses

Used in Pharmaceutical Industry:
.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate is used as a potential pharmaceutical compound for [application reason] due to its unique molecular structure and the presence of the anhydro-3-deoxy-4-O group, which may offer specific biological activities or interactions with biological targets.
Used in Chemical Research:
In the field of chemical research, .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate is used as a research tool for [application reason], such as studying carbohydrate chemistry, investigating the effects of the phenylmethyl modification on compound properties, or exploring its potential as a precursor in the synthesis of other complex molecules.
Used in Material Science:
Within the material science industry, .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate is used as a component in the development of [application type] for [application reason], possibly due to its unique structural features that could contribute to the creation of novel materials with specific properties.

Check Digit Verification of cas no

The CAS Registry Mumber 102719-12-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,1 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102719-12:
(8*1)+(7*0)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*2)=90
90 % 10 = 0
So 102719-12-0 is a valid CAS Registry Number.

102719-12-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-O-acetyl-1,6-anhydro-4-O-benzyl-3-deoxy-β-D-arabino-hexopyranose

1.2 Other means of identification

Product number -
Other names Acetic acid (1R,2S,4S,5R)-2-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:102719-12-0 SDS

102719-12-0Relevant articles and documents

SYNTHESIS AND THERMAL CHEMISTRY OF ISOLEVOGLUCOSENONE

Furneaux, Richard H.,Gainsford, Graeme J.,Shafizadeh, Fred,Stevenson, Thomas T.

, p. 113 - 128 (2007/10/02)

Isolevoglucosenone (1,6-anhydro-2,3-dideoxy-β-D-glycero-hex-2-enopyranos-4-ulose, 3) has been synthesized from levoglucosenone (2) in six steps.Thus, 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose, obtained by Michael addition of benzyl al

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