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3-iodo-1-phenyl-1H-pyrazole is a heterocyclic aromatic compound with the molecular formula C9H7IN2. It features a pyrazole ring fused with an iodine atom and a phenyl group, making it a versatile building block in organic synthesis and medicinal chemistry for the development of complex molecules. Its unique structure allows it to participate in a wide range of chemical transformations, which is highly valuable for researchers and chemists in their quest to create novel compounds and pharmaceuticals.

141998-90-5

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141998-90-5 Usage

Uses

Used in Organic Synthesis:
3-iodo-1-phenyl-1H-pyrazole is used as a building block in organic synthesis for the creation of more complex molecules. Its pyrazole ring and attached functional groups enable the formation of various derivatives, which can be further modified to obtain desired properties and functionalities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-iodo-1-phenyl-1H-pyrazole is utilized as a key component in the design and synthesis of potential pharmaceuticals. Its ability to participate in diverse chemical transformations allows for the development of new drug candidates with improved therapeutic properties and selectivity.
Used in Chemical Reactions:
3-iodo-1-phenyl-1H-pyrazole serves as a reagent in various chemical reactions, such as halogenation and Suzuki-Miyaura cross-coupling reactions. Its presence in these reactions facilitates the formation of new chemical bonds and the synthesis of novel compounds with potential applications in various industries.
Used in Research and Development:
As a valuable tool for researchers and chemists, 3-iodo-1-phenyl-1H-pyrazole is employed in the exploration of new chemical pathways and the discovery of innovative compounds. Its versatility in participating in different chemical transformations makes it an essential component in the pursuit of groundbreaking advancements in the fields of chemistry and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 141998-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,9 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141998-90:
(8*1)+(7*4)+(6*1)+(5*9)+(4*9)+(3*8)+(2*9)+(1*0)=165
165 % 10 = 5
So 141998-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H9IN2/c11-10-6-12-13(8-10)7-9-4-2-1-3-5-9/h1-6,8H,7H2

141998-90-5SDS

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 4-Iodo-1-phenyl-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 3-iodo-1-methyl-1Hpyrazolo[3,4-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:141998-90-5 SDS

141998-90-5Downstream Products

141998-90-5Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS AND USE OF SAME

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Paragraph 00226, (2016/01/08)

Novel heterocyclic compounds are provided which display useful efficacy in the treatment of diseases caused by trypanosomatids. Particularly, the compounds of the invention are useful in the treatment of HAT and/or Chagas disease and/or Animal African trypanosomiasis (AAT).

SYNTHESIS AND REACTION OF TRIBUTYLSTANNYLPYRAZOLES

Sakamoto, Takao,Shiga, Futoshi,Uchiyama, Daishi,Kondo, Yoshinori,Yamanaka, Hiroshi

, p. 813 - 818 (2007/10/02)

1,3-Dipolar cycloaddition reaction of diazomethane and ethyl diazoacetate with tributylstannylacetylenes occurred regioselectively to afford the corresponding 3(5)-tributylstannylpyrazoles.The cycloaddition reaction of 3-phenylsydnone with the stannylacetylenes proceeded also regioselectively, and 3-tributylstannyl-1-phenylpyrazoles were isolated. 4-Tributylstannyl- and 5-tributylstannyl-1-phenylpyrazole were prepared by the stannylation of 4-lithio- and 5-lithio-1-phenylpyrazoles with tributylstannyl chloride.Iodination, benzoylation, and phenylation of the stannylpyrazoles were examined.

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