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(3aR,4R,6aR)-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-ol is a complex organic compound characterized by its unique molecular structure. It belongs to the class of chemicals known as dioxolanes, which are heterocyclic compounds containing both oxygen and carbon atoms in their ring structure. This specific compound features a tetrahydrofuran ring fused to a dioxolane ring, with two methyl groups attached to the carbon at position 2. The stereochemistry at positions 3a, 4, and 6a is crucial, as it determines the compound's biological activity and physical properties. This chemical is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or materials science, although specific uses are not detailed here.

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  • 90409-96-4 Structure
  • Basic information

    1. Product Name: (3aR,4R,6aR)-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-ol
    2. Synonyms: (3aR,4R,6aR)-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-ol
    3. CAS NO:90409-96-4
    4. Molecular Formula:
    5. Molecular Weight: 160.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90409-96-4.mol
    9. Article Data: 2
  • 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: (3aR,4R,6aR)-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3aR,4R,6aR)-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-ol(90409-96-4)
    11. EPA Substance Registry System: (3aR,4R,6aR)-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-ol(90409-96-4)
  • 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: 90409-96-4(Hazardous Substances Data)

90409-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90409-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,0 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90409-96:
(7*9)+(6*0)+(5*4)+(4*0)+(3*9)+(2*9)+(1*6)=134
134 % 10 = 4
So 90409-96-4 is a valid CAS Registry Number.

90409-96-4Relevant articles and documents

Synthesis of dl-cis-and (4R,5R)-trans-7--5(Z)-heptenoic acid analogues as platelet thromboxane A2 receptor antagonists

Komiotis, D.,Pananookooln, S.,Zaw, K.,Dieter, J. P.,Breton, G. C. Le,Venton, D. L.

, p. 321 - 326 (2007/10/02)

The title compounds have been synthesized and their in vitro thromboxane A2(TxA2) receptor antagonist activity evaluated.Both cis and trans isomers (1,2) were shown to specifically inhibit submaximal human platelet aggregation induced by 225 nM U46619 in a dose-dependent manner with an IC50 of 1 μM.The concentration of 1 and 2 required to completely block maximal aggregation induced by 3 μM U46619 was 3 μM. thromboxane A2/ receptor antagonist/ platelet aggregation/ 1,3-dioxolane

Aldol Reaction between Small Sugars. Preparation of DL-threo-2-Pentulose and DL-lyxo-3-Hexulose and their Isolation as O-Isopropylidene Derivatives

Morgenlie, Svein

, p. 745 - 748 (2007/10/02)

The improved diastereoselectivity obtained with strongly basic anion-exchange resin as catalyst in aldol condensation between two-, three- and four-carbon "sugars" has been utilised in the preparation of DL-threo-2-pentulose and DL-lyxo-3-hexulose, which were isolated as their O-isopropylidene derivatives.A possible reason for the observe preference of formation of the lyxo-diastereomer in condensation between glycolaldehyde and glycero-tetrulose is suggested.

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