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937251-02-0

3,6-anhydro-2-deoxy-4,5-O-isopropylidene-1-O-(methylsulfonyl)-7-O-trityl-D-allo-heptitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 937251-02-0 Structure

  • Basic information

    1. Product Name: 3,6-anhydro-2-deoxy-4,5-O-isopropylidene-1-O-(methylsulfonyl)-7-O-trityl-D-allo-heptitol
    2. Synonyms: 3,6-anhydro-2-deoxy-4,5-O-isopropylidene-1-O-(methylsulfonyl)-7-O-trityl-D-allo-heptitol
    3. CAS NO:937251-02-0
    4. Molecular Formula:
    5. Molecular Weight: 538.662
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 937251-02-0.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: 3,6-anhydro-2-deoxy-4,5-O-isopropylidene-1-O-(methylsulfonyl)-7-O-trityl-D-allo-heptitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,6-anhydro-2-deoxy-4,5-O-isopropylidene-1-O-(methylsulfonyl)-7-O-trityl-D-allo-heptitol(937251-02-0)
    11. EPA Substance Registry System: 3,6-anhydro-2-deoxy-4,5-O-isopropylidene-1-O-(methylsulfonyl)-7-O-trityl-D-allo-heptitol(937251-02-0)

  • 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: 937251-02-0(Hazardous Substances Data)

937251-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 937251-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,7,2,5 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 937251-02:
(8*9)+(7*3)+(6*7)+(5*2)+(4*5)+(3*1)+(2*0)+(1*2)=170
170 % 10 = 0
So 937251-02-0 is a valid CAS Registry Number.

937251-02-0Relevant articles and documents

Synthesis and biochemical evaluation of guanidino-alkyl-ribitol derivatives as nucleoside hydrolase inhibitors

Goeminne,McNaughton,Bal,Surpateanu,Van Der Veken,De Prol,Versees,Steyaert,Haemers,Augustyns

, p. 315 - 326 (2008/09/18)

Nucleoside hydrolase (NH) is a key enzyme in the purine salvage pathway. The purine specificity of the IAG-NH from Trypanosoma vivax is at least in part due to cation-π-stacking interactions. Guanidinium ions can be involved in cation-π-stacking interactions, therefore a series of guanidino-alkyl-ribitol derivatives were synthesized in order to examine the binding affinity of these compounds towards the target enzyme. The compounds show moderate to good inhibiting activity towards the IAG-NH from T. vivax.

1,2,3-Triazolylalkylribitol derivatives as nucleoside hydrolase inhibitors

Goeminne,McNaughton,Bal,Surpateanu,Van der Veken,De Prol,Versees,Steyaert,Apers,Haemers,Augustyns

, p. 2523 - 2526 (2008/02/05)

A range of novel 1,2,3-triazolylalkylribitol derivatives were synthesized and evaluated as nucleoside hydrolase inhibitors. The most active compound (11a) has low micromolar potency and is structurally diverse from previously reported nucleoside hydrolase

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