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CAS

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161924-07-8

2-(methoxycarbonyl)oxy-1-benzyloxy-2-benzyloxymethyl-3-butyne is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 161924-07-8 Structure

  • Basic information

    1. Product Name: 2-(methoxycarbonyl)oxy-1-benzyloxy-2-benzyloxymethyl-3-butyne
    2. Synonyms:
    3. CAS NO:161924-07-8
    4. Molecular Formula:
    5. Molecular Weight: 354.403
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 161924-07-8.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: 2-(methoxycarbonyl)oxy-1-benzyloxy-2-benzyloxymethyl-3-butyne(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(methoxycarbonyl)oxy-1-benzyloxy-2-benzyloxymethyl-3-butyne(161924-07-8)
    11. EPA Substance Registry System: 2-(methoxycarbonyl)oxy-1-benzyloxy-2-benzyloxymethyl-3-butyne(161924-07-8)

  • 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: 161924-07-8(Hazardous Substances Data)

161924-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161924-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,2 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 161924-07:
(8*1)+(7*6)+(6*1)+(5*9)+(4*2)+(3*4)+(2*0)+(1*7)=128
128 % 10 = 8
So 161924-07-8 is a valid CAS Registry Number.

161924-07-8Relevant articles and documents

Alkylation of Adenine with Functionalized tert.-Propargyl Carbonates. Synthesis of 3'-Hydroxymethyladenallene - a New Analogue of 2'-Deoxyadenosine

Xu, Ze-Qi,Joshi, Ramachandra V.,Zemlicka, Jiri

, p. 67 - 76 (2007/10/02)

Esters 9d - 9g derived from acetylenic carbinol 5 were prepared and they were studied as potential alkylating agents with adenine (10), N6-benzoyl- and N6-dimethylamino-methyleneadenine (16 and 17).Carbonates 9f and 9g were the most suitable giving allene 11 and acetylene 12 (after N-deprotection in case of 16 and 17).On a scale larger than 0.2 mmol, slow addition of carbonate 9f or 9g to a solution of 10, 16 or 17 in DMF at 60 degC was most conducive to formation of allenic derivative 11.Such conditions also supperessed formation of by-products such as carbonate 13a and N9-methyladenine (14) observed in the case of methyl carbonate 9f.Intermediates 11 and 12 were deprotected using BCl3 in CH2Cl2 to give 3'-hydroxymethyladenallene (4a) and diol 15, respectively.Compound 4a was deaminated with adenosine deaminase.

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