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ETHYL 4-CHLORO-5H-PYRROLO[3,2-D]PYRIMIDINE-7-CARBOXYLATE is a chemical compound with the molecular formula C11H9ClN4O2, belonging to the class of organic compounds known as pyrrolopyrimidines. It is a derivative of pyrrolopyrimidine and is commonly used in medicinal chemistry and pharmaceutical research due to its potential biological activities, such as antitumor and antimicrobial properties. The ethyl ester group in its structure makes it suitable for use in organic synthesis and drug formulation, making it a valuable tool in drug discovery and development.

853058-42-1

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853058-42-1 Usage

Uses

Used in Pharmaceutical Research:
ETHYL 4-CHLORO-5H-PYRROLO[3,2-D]PYRIMIDINE-7-CARBOXYLATE is used as a research compound for its potential antitumor and antimicrobial properties. Its unique chemical structure and biological activities make it a promising candidate for the development of new drugs to treat various diseases.
Used in Organic Synthesis:
ETHYL 4-CHLORO-5H-PYRROLO[3,2-D]PYRIMIDINE-7-CARBOXYLATE is used as a key intermediate in the synthesis of various organic compounds. Its ethyl ester group allows for further chemical modifications and functionalization, enabling the development of new molecules with potential applications in various fields.
Used in Drug Formulation:
ETHYL 4-CHLORO-5H-PYRROLO[3,2-D]PYRIMIDINE-7-CARBOXYLATE is used as a pharmaceutical excipient in drug formulation. Its compatibility with other drug components and its ability to improve drug solubility and stability make it a valuable ingredient in the development of effective drug formulations.
Used in Drug Discovery:
ETHYL 4-CHLORO-5H-PYRROLO[3,2-D]PYRIMIDINE-7-CARBOXYLATE is used as a lead compound in drug discovery. Its unique chemical properties and potential biological activities provide a foundation for the design and optimization of new drugs with improved therapeutic effects and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 853058-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,0,5 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 853058-42:
(8*8)+(7*5)+(6*3)+(5*0)+(4*5)+(3*8)+(2*4)+(1*2)=171
171 % 10 = 1
So 853058-42-1 is a valid CAS Registry Number.

853058-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-chloro-5H-pyrrolo[3,2-d]pyrimidine-7-carboxylate

1.2 Other means of identification

Product number -
Other names 4-chloro-5H-pyrrolo[3,2-d]pyrimidine-7-carboxylic acid ethyl ester

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:853058-42-1 SDS

853058-42-1Relevant articles and documents

Inhibitors of HIV-1 attachment. Part 11: The discovery and structure-activity relationships associated with 4,6-diazaindole cores

Bender, John A.,Yang, Zhong,Eggers, Betsy,Gong, Yi-Fei,Lin, Pin-Fang,Parker, Dawn D.,Rahematpura, Sandhya,Zheng, Ming,Meanwell, Nicholas A.,Kadow, John F.

, p. 218 - 222 (2013/02/23)

A series of HIV-1 attachment inhibitors containing a 4,6-diazaindole core were examined in an effort to identify a compound which improved upon the potency and oral exposure of BMS-488043 (2). BMS-488043 (2) is a 6-azaindole-based HIV-1 attachment inhibit

RAF INHIBITOR COMPOUNDS AND METHODS OF USE THEREOF

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Page/Page column 85, (2011/04/14)

Compounds of Formula I are useful for inhibition of Raf kinases. Methods of using compounds of Formula I and stereoisomers, tautomers, prodrugs and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or trea

The efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride

Ham, Young Jin,Lee, Duck-Hyung,Choi, Hwan Geun,Hah, Jung-Mi,Sim, Taebo

experimental part, p. 4609 - 4611 (2010/09/18)

A facile one-step transformation of methylsulfanyl and arylsulfanyl groups on pyrimidine ring system into the corresponding chloride group was achieved using sulfuryl chloride in acetonitrile/dichloromethane.

Diazaindole-dicarbonyl-piperazinyl antiviral agents

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Page/Page column 44, (2008/06/13)

The invention comprises substituted diazaindole-dicarbonyl-piperazinyl derivatives of general Formula I wherein: Q is selected from the group consisting of — may represent a bond; T is —C(O)— or —CH(CN)—; and —Y— is selected from the group consisting of compositions thereof and their use for treating HIV infection.

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