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CAS

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227079-07-4

1,5-anhydro-3-O-benzoyl-2-deoxy-2-(N4-benzoylcytosin-1-yl)-D-altro-hexitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 227079-07-4 Structure

  • Basic information

    1. Product Name: 1,5-anhydro-3-O-benzoyl-2-deoxy-2-(N4-benzoylcytosin-1-yl)-D-altro-hexitol
    2. Synonyms:
    3. CAS NO:227079-07-4
    4. Molecular Formula:
    5. Molecular Weight: 465.463
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 227079-07-4.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: 1,5-anhydro-3-O-benzoyl-2-deoxy-2-(N4-benzoylcytosin-1-yl)-D-altro-hexitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,5-anhydro-3-O-benzoyl-2-deoxy-2-(N4-benzoylcytosin-1-yl)-D-altro-hexitol(227079-07-4)
    11. EPA Substance Registry System: 1,5-anhydro-3-O-benzoyl-2-deoxy-2-(N4-benzoylcytosin-1-yl)-D-altro-hexitol(227079-07-4)

  • 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: 227079-07-4(Hazardous Substances Data)

227079-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 227079-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,0,7 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 227079-07:
(8*2)+(7*2)+(6*7)+(5*0)+(4*7)+(3*9)+(2*0)+(1*7)=134
134 % 10 = 4
So 227079-07-4 is a valid CAS Registry Number.

227079-07-4Relevant articles and documents

Synthesis of protected D-altritol nucleosides as building blocks for oligonucleotide synthesis

Allart, Brigitte,Busson, Roger,Rozenski, Jef,Van Aerschot, Arthur,Herdewijn, Piet

, p. 6527 - 6546 (2007/10/03)

D-Altritol nucleosides with an adenine and uracil base moiety were obtained by nucleophilic opening of the epoxide ring of 1,5:2,3-dianhydro- 4,6-O-benzylidene-D-allitol using the sodium salt of the above mentioned bases. The use of a 2-trimethylsilylethyl protecting group for the O6- function of the guanine base offers a useful compromise between stability and acceptable alkylation yields of the N9-position if the guanine base. The cytosine nucleoside was synthesized starting from the uracil congener. The 3'-hydroxyl function was protected with a benzoyl group.

1,5-Anhydro-2-deoxy-D-altritol oligonucleotides as conformationally restricted analogues of RNA

Allart, Brigitte,Van Aerschot, Arthur,Herdewijn, Piet

, p. 1523 - 1526 (2007/10/03)

As part of a project concerning the investigation of new hexitol nucleic acids (HNA), the 1,5-anhydro-2-deoxy-D-altritol nucleoside building blocks with a uracil, cytosine, adenine and guanine base moiety were synthesized. The uracil analogue was used for the automated synthesis of corresponding oligonucleotides. Hybridization capabilities of these altritol nucleic acids (ANA) are illustrated by the Tm values obtained for the (d(h)U)13/(dA)13 duplex.

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