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1H-Pyrrolo[2,3-b]pyridine, 4-chloro-2-iodois a heterocyclic chemical compound with the molecular formula C8H5ClIN. It features a pyrrolo-pyridine core structure, with a chlorine atom at the 4-position and an iodine atom at the 2-position. 1H-Pyrrolo[2,3-b]pyridine, 4-chloro-2-iodois known for its unique reactivity due to the presence of both halogen atoms, making it a valuable intermediate in the synthesis of a wide range of organic compounds and pharmaceuticals.

940948-29-8

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940948-29-8 Usage

Uses

Used in Pharmaceutical Industry:
1H-Pyrrolo[2,3-b]pyridine, 4-chloro-2-iodois used as a building block for the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
1H-Pyrrolo[2,3-b]pyridine, 4-chloro-2-iodois used as a key intermediate in the production of agrochemicals. Its versatile chemical properties enable the creation of novel compounds with potential applications in crop protection and pest control.
Used in Chemical Research:
1H-Pyrrolo[2,3-b]pyridine, 4-chloro-2-iodoserves as a useful reagent in chemical research and organic synthesis. Its presence in various chemical reactions aids in the exploration of new synthetic pathways and the development of innovative chemical compounds.
Used in Organic Synthesis:
1H-Pyrrolo[2,3-b]pyridine, 4-chloro-2-iodois utilized as a starting material in the synthesis of diverse organic compounds. Its unique structure and reactivity contribute to the formation of a wide array of chemical products with various applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 940948-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,0,9,4 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 940948-29:
(8*9)+(7*4)+(6*0)+(5*9)+(4*4)+(3*8)+(2*2)+(1*9)=198
198 % 10 = 8
So 940948-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClIN2/c8-5-1-2-10-7-4(5)3-6(9)11-7/h1-3H,(H,10,11)

940948-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-2-iodo-7-azaindole

1.2 Other means of identification

Product number -
Other names 4-chloro-2-iodo-1H-pyrrolo[2,3-b]pyridine

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:940948-29-8 SDS

940948-29-8Relevant academic research and scientific papers

COMPOUNDS FOR USING IN IMAGING AND PARTICULARLY FOR THE DIAGNOSIS OF NEURODEGENERATIVE DISEASES

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Paragraph 0578; 0579; 0609; 0618; 0619; 0640; 0641, (2019/07/23)

The invention relates to compounds of formula (II) for using in imaging and particularly for the diagnosis of neurodegenerative diseases

Discovery of N-substituted 7-azaindoles as PIM1 kinase inhibitors – Part I

Barberis, Claude,Moorcroft, Neil,Arendt, Chris,Levit, Mikhail,Moreno-Mazza, Sandra,Batchelor, Joseph,Mechin, Ingrid,Majid, Tahir

, p. 4730 - 4734 (2017/09/27)

Novel N-substituted azaindoles have been discovered as PIM1 inhibitors. X-ray structures have played a significant role in orienting the chemistry effort in the initial phase of hit confirmation. Disclosure of an unconventional binding mode for 1 and 2, as demonstrated by X-ray crystallography, is presented and was an important factor in selecting and advancing a lead series.

AZAINDOLE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION

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, (2011/07/07)

The disclosure relates generally to compounds that inhibit Pim kinases. Provided herein are N-substituted azaindoles, or pharmaceutically acceptable salts thereof, which are useful as selective inhibitors of Pim kinases. The disclosure also relates to pharmaceutical compositions comprising these compounds, processes for their preparation, and methods of using the same.

Pyrrolopyridine kinase inhibiting compounds

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Page/Page column 80, (2010/11/27)

Compounds represented by Formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, are inhibitors of least one of the Abl, Aurora-A, Blk, c-Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mek1, PDK-1, GSK3β, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, IGF-1R, Ron, Met, and KDR kinases in animals, including humans, for the treatment and/or prevention of various diseases and conditions such as cancer.

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