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4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine, also known as CPP, is a heterocyclic organic compound with a molecular formula of C7H4N4. It features a pyrrolopyrimidine core with a cyano group attached at the 4th position, making it a versatile building block in the synthesis of pharmaceuticals and other organic compounds. Known for its potential antimicrobial, antiviral properties, and its ability to modulate ion channels and receptors in the central nervous system, CPP has emerged as a promising candidate for various medicinal and industrial applications.

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  • 1005206-16-5 Structure
  • Basic information

    1. Product Name: 4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine
    2. Synonyms: 4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine;7H-Pyrrolo[2,3-d]pyriMidine-4-carbonitrile
    3. CAS NO:1005206-16-5
    4. Molecular Formula: C7H4N4
    5. Molecular Weight: 144.13346
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1005206-16-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.44
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 10.25±0.50(Predicted)
    10. CAS DataBase Reference: 4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine(1005206-16-5)
    12. EPA Substance Registry System: 4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine(1005206-16-5)
  • 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: 1005206-16-5(Hazardous Substances Data)

1005206-16-5 Usage

Uses

Used in Pharmaceutical Research and Development:
4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Antimicrobial Applications:
4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine is used as an antimicrobial agent for its potential to inhibit the growth of bacteria and other microorganisms. Its ability to target specific cellular processes makes it a valuable tool in the fight against antibiotic-resistant strains.
Used in Antiviral Applications:
4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine is used as an antiviral agent, leveraging its ability to interfere with viral replication and assembly. This property makes it a promising candidate for the development of new antiviral therapies.
Used in Modulation of Ion Channels and Receptors:
4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine is used as a modulator of ion channels and receptors in the central nervous system. Its interaction with these targets can lead to the development of treatments for neurological disorders and conditions.
Used in Organic Synthesis:
4-Cyano-7H-Pyrrolo[2,3-d]pyrimidine is used as a precursor in organic synthesis to produce more complex chemical structures. Its versatility in forming various derivatives makes it an essential component in the creation of advanced materials and compounds for diverse applications across industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1005206-16-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,5,2,0 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1005206-16:
(9*1)+(8*0)+(7*0)+(6*5)+(5*2)+(4*0)+(3*6)+(2*1)+(1*6)=75
75 % 10 = 5
So 1005206-16-5 is a valid CAS Registry Number.
InChI:InChI=1S/C7H4N4/c8-3-6-5-1-2-9-7(5)11-4-10-6/h1-2,4H,(H,9,10,11)

1005206-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7H-Pyrrolo[2,3-d]pyrimidine-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 7H-pyrrolo[2,3-d]pyrimidine-4-carbonitrile

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:1005206-16-5 SDS

1005206-16-5Relevant articles and documents

PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES AS CGRP RECEPTOR ANTAGONISTS

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Page/Page column 72-73, (2009/07/25)

The present invention relates to novel compounds that are CGRP receptor antagonists, processes for their preparation, to compositions containing them and to their use in the treatment of migraine, headache, and cluster headache.

PROTEIN KINASE INHIBITORS AND METHODS FOR USING THEREOF

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Page/Page column 52, (2009/01/20)

The invention provides compounds of formula (l) and pharmaceutical compositions thereof, which are useful as protein kinase inhibitors, and methods for using such compounds to treat, ameliorate or prevent a condition associated with abnormal or deregulated kinase activity. In some embodiments, the invention provides methods for using such compounds to treat, ameliorate or prevent diseases or disorders that involve abnormal activation of AIk, AbI, Aurora-A, B-Raf, C-Raf, Bcr-Abl, BRK, BIk, Bmx, BTK, c-Kit, c-RAF, CSK, c-SRC, EphBl, EphB2, EphB4, FLTl, Fms, Flt3, Fyn, FRK3, JAK2, KDR, Lck, Lyn, PDGFRalpha, PDGFRbeta, PKCalpha, SAPK2alpha, Src, SIK, Syk, Tie2 and TrkB kinases.

COMPOUNDS AND METHODS OF USE

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Page/Page column 129, (2010/11/27)

Selected compounds are effective for prophylaxis and treatment of diseases, such as angiogenesis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.

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