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873792-93-9

5-BROMO-4-CHLORO-7-SS-D-RIBOFURANOSYL-7H-PYRROLO[2,3-D]PYRIMIDIN-2-AMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 873792-93-9 Structure

  • Basic information

    1. Product Name: 5-BROMO-4-CHLORO-7-SS-D-RIBOFURANOSYL-7H-PYRROLO[2,3-D]PYRIMIDIN-2-AMINE
    2. Synonyms: 5-BROMO-4-CHLORO-7-SS-D-RIBOFURANOSYL-7H-PYRROLO[2,3-D]PYRIMIDIN-2-AMINE
    3. CAS NO:873792-93-9
    4. Molecular Formula: C11H12BrClN4O4
    5. Molecular Weight: 379.597
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 873792-93-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-BROMO-4-CHLORO-7-SS-D-RIBOFURANOSYL-7H-PYRROLO[2,3-D]PYRIMIDIN-2-AMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-BROMO-4-CHLORO-7-SS-D-RIBOFURANOSYL-7H-PYRROLO[2,3-D]PYRIMIDIN-2-AMINE(873792-93-9)
    11. EPA Substance Registry System: 5-BROMO-4-CHLORO-7-SS-D-RIBOFURANOSYL-7H-PYRROLO[2,3-D]PYRIMIDIN-2-AMINE(873792-93-9)

  • 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: 873792-93-9(Hazardous Substances Data)

873792-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 873792-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,7,9 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 873792-93:
(8*8)+(7*7)+(6*3)+(5*7)+(4*9)+(3*2)+(2*9)+(1*3)=229
229 % 10 = 9
So 873792-93-9 is a valid CAS Registry Number.

873792-93-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7H-Pyrrolo[2,3-d]pyrimidin-2-amine, 5-bromo-4-chloro-7-β-D-ribofuranosyl-

1.2 Other means of identification

Product number -
Other names 5-BROMO-4-CHLORO-7-SS-D-RIBOFURANOSYL-7H-PYRROLO[2,3-D]PYRIMIDIN-2-AMINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:873792-93-9 SDS

873792-93-9Downstream Products

873792-93-9Relevant articles and documents

7-Deazapurin-2,6-diamine and 7-deazaguanine: Synthesis and property of 7-substituted nucleosides and oligonucleotides

Seela, Frank,Peng, Xiaohua,Ming, Xin

, p. 839 - 841 (2005)

The synthesis of 7-substituted 7-deazaguanine and 7-deazaadenine ribonucleosides 1-2, the incorporation of 3a-d into oligonucleotides, and the stability of the corresponding duplexes and base discrimination are described. The pKa values of 3-4

C6–O-alkylated 7-deazainosine nucleoside analogues: Discovery of potent and selective anti-sleeping sickness agents

Hulpia, Fabian,Bouton, Jakob,Campagnaro, Gustavo D.,Alfayez, Ibrahim A.,Mabille, Dorien,Maes, Louis,de Koning, Harry P.,Caljon, Guy,Van Calenbergh, Serge

, (2020/01/13)

African trypanosomiasis, a deadly infectious disease caused by the protozoan Trypanosoma brucei spp., is spread to new hosts by bites of infected tsetse flies. Currently approved therapies all have their specific drawbacks, prompting a search for novel th

7-Functionalized 7-deazapurine ribonucleosides related to 2-aminoadenosine, guanosine, and xanthosine: Glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose

Seela, Frank,Peng, Xiaohua

, p. 81 - 90 (2007/10/03)

The Silyl-Hilbert-Johnson reaction as well as the nucleobase-anion glycosylation of a series of 7-deazapurines has been investigated, and the 7-functionalized 7-deazapurine ribonucleosides were prepared. Glycosylation of the 7-halogenated 6-chloro-2-pival

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