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91121-19-6

1,2-dideoxyribose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91121-19-6 Structure

  • Basic information

    1. Product Name: 1,2-dideoxyribose
    2. Synonyms: 1,2-dideoxyribose;2-Furanmethanol, tetrahydro-3-hydroxy-, trans-;trans-Tetrahydro-3-hydroxy-2-furanmethanol
    3. CAS NO:91121-19-6
    4. Molecular Formula: C5H10O3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91121-19-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 275.1°Cat760mmHg
    3. Flash Point: 120.2°C
    4. Appearance: /
    5. Density: 1.239g/cm3
    6. Vapor Pressure: 0.000657mmHg at 25°C
    7. Refractive Index: 1.496
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,2-dideoxyribose(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2-dideoxyribose(91121-19-6)
    12. EPA Substance Registry System: 1,2-dideoxyribose(91121-19-6)

  • 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: 91121-19-6(Hazardous Substances Data)

91121-19-6 Usage

Explanation

Also known as 2-deoxyribose, it is a modified form of the sugar ribose.

Explanation

This modification distinguishes 1,2-dideoxyribose from ribose.

Explanation

The absence of the 2'-hydroxyl group makes 1,2-dideoxyribose a crucial part of DNA nucleotides.

Explanation

1,2-dideoxyribose is used in the development of antiviral and anticancer drugs through the synthesis of nucleoside analogs.

Explanation

1,2-dideoxyribose is used as a substrate in enzymatic glycosylation reactions for the production of oligosaccharides and glycoconjugates.

Explanation

The importance of 1,2-dideoxyribose lies in its role in the structure and function of nucleotides, its utility in the development of pharmaceuticals, and its use in the synthesis of complex carbohydrates.

Structural difference

Lacks the 2'-hydroxyl group

Role in nucleotides

Important component of DNA

Application in pharmaceuticals

Synthesis of nucleoside analogs

Enzymatic glycosylation

Common substrate

Significance

Nucleotide structure and function, pharmaceutical development, and complex carbohydrate synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 91121-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,2 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91121-19:
(7*9)+(6*1)+(5*1)+(4*2)+(3*1)+(2*1)+(1*9)=96
96 % 10 = 6
So 91121-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O3/c6-3-5-4(7)1-2-8-5/h4-7H,1-3H2/t4-,5+/m0/s1

91121-19-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(hydroxymethyl)oxolan-3-ol

1.2 Other means of identification

Product number -
Other names 1,4-anhydro-2-deoxy-D-erythro-pentitol

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:91121-19-6 SDS

91121-19-6Downstream Products

91121-19-6Relevant articles and documents

Biomimetic cyclisation of prebrevetoxin polyepoxide models

Kelly, David R.,Nally, James

, p. 3251 - 3254 (2007/10/03)

(E)-1,3-Dihydroxyhex-4-ene and (E)-1,3-dihydroxy-4-methylhex-4-ene undergo epoxidation with peracetic acid and in situ cyclisation to give a mixture of tetrahydro-furans and -pyrans, whereas comparable compounds lacking the allylic hydroxyl group give pre

P(V) trigonal bipyramidal phosphoranes as model compounds for the description of cAMP-catalyzed reactions

Ool, Peter J. J. M. van,Buck, Henk M.

, p. 119 - 122 (2007/10/02)

13C NMR low-temperature investigations have revealed that the dioxaphospharinane ring, trans-annelated with a cyclopentane ring (3), prefers an equatorial-apical alignment in trigonal bipyramidal phosphoranes.However, the 13C NMR low-temperature investigations of the model compound, in which the dioxaphospharinane ring is trans-annelated with a tetrahydrofuran ring (4), have shown that the ligand exchange (pseudorotation) in this compound is very fast on the NMR time scale, even at low temperature.These results are in fairly good agreement with quantum-chemical calculations.

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