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1446175-09-2

2,4-bis-benzyloxy-5-N-boc-7-iodopyrrolo[3,2-d]pyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446175-09-2 Structure

  • Basic information

    1. Product Name: 2,4-bis-benzyloxy-5-N-boc-7-iodopyrrolo[3,2-d]pyrimidine
    2. Synonyms: 2,4-bis-benzyloxy-5-N-boc-7-iodopyrrolo[3,2-d]pyrimidine
    3. CAS NO:1446175-09-2
    4. Molecular Formula:
    5. Molecular Weight: 557.388
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446175-09-2.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: 2,4-bis-benzyloxy-5-N-boc-7-iodopyrrolo[3,2-d]pyrimidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-bis-benzyloxy-5-N-boc-7-iodopyrrolo[3,2-d]pyrimidine(1446175-09-2)
    11. EPA Substance Registry System: 2,4-bis-benzyloxy-5-N-boc-7-iodopyrrolo[3,2-d]pyrimidine(1446175-09-2)

  • 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: 1446175-09-2(Hazardous Substances Data)

1446175-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446175-09-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,1,7 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1446175-09:
(9*1)+(8*4)+(7*4)+(6*6)+(5*1)+(4*7)+(3*5)+(2*0)+(1*9)=162
162 % 10 = 2
So 1446175-09-2 is a valid CAS Registry Number.

1446175-09-2Downstream Products

1446175-09-2Relevant articles and documents

Antiproliferative activities of halogenated pyrrolo[3,2-d]pyrimidines

Temburnikar, Kartik W.,Ross, Christina R.,Wilson, Gerald M.,Balzarini, Jan,Cawrse, Brian M.,Seley-Radtke, Katherine L.

, p. 4354 - 4363 (2015)

In vitro evaluation of the halogenated pyrrolo[3,2-d]pyrimidines identified antiproliferative activities in compounds 1 and 2 against four different cancer cell lines. Upon screening of a series of pyrrolo[3,2-d]pyrimidines, the 2,4-Cl compound 1 was foun

Synthesis of 2′-deoxy-9-deaza nucleosides using heck methodology

Temburnikar, Kartik,Brace, Kelin,Seley-Radtke, Katherine L.

, p. 7305 - 7311 (2013/08/23)

During the synthesis of a series of 2′-deoxy-9-deaza nucleosides using Heck methodology, the necessity for a pyrrole protecting group was discovered. The results of this brief study revealed that the benzyloxymethyl (BOM) group proved optimal, and Heck coupling using Jeffery conditions increased the coupling yield significantly. The results are reported herein.

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