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1-(4-Iodo-phenyl)-2-methyl-1H-imidazole is a heterocyclic aromatic organic compound with the molecular formula C9H8IN3. It features an imidazole ring with a 4-iodo-phenyl group and a methyl group attached, making it a white to off-white crystalline solid that is slightly soluble in water and soluble in organic solvents.

179420-75-8

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179420-75-8 Usage

Uses

Used in Medicinal Chemistry:
1-(4-Iodo-phenyl)-2-methyl-1H-imidazole is used as a building block for the development of pharmaceutical drugs due to its potential pharmacological properties.
Used in Organic Synthesis:
1-(4-Iodo-phenyl)-2-methyl-1H-imidazole is also utilized in organic synthesis, serving as a key intermediate for the creation of various organic compounds.
Used in Chemical Research and Development:
1-(4-Iodo-phenyl)-2-methyl-1H-imidazole may be employed in the field of chemical research and development for exploring its properties and applications further.

Check Digit Verification of cas no

The CAS Registry Mumber 179420-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,4,2 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 179420-75:
(8*1)+(7*7)+(6*9)+(5*4)+(4*2)+(3*0)+(2*7)+(1*5)=158
158 % 10 = 8
So 179420-75-8 is a valid CAS Registry Number.

179420-75-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-iodophenyl)-2-methylimidazole

1.2 Other means of identification

Product number -
Other names -

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:179420-75-8 SDS

179420-75-8Relevant academic research and scientific papers

Optimization of imidazole 5-lipoxygenase inhibitors and selection and synthesis of a development candidate

Mano, Takashi,Stevens, Rodney W.,Ando, Kazuo,Kawai, Makoto,Kawamura, Kiyoshi,Nakao, Kazunari,Okumura, Yoshiyuki,Okumura, Takako,Sakakibara, Minoru,Miyamoto, Kimitaka,Tamura, Tetsuya

, p. 965 - 973 (2007/10/03)

Structural modification of imidazole 5-lipoxygenase (5-LO) inhibitors for optimizing inhibitory potency, pharmacokinetic behavior and toxicity (ocular) profile led to 4-{3-[4-(2-methyl-1H-imidazol-1-yl)phenylthio]}phenyl-3,4,5,6- tetrahydro-2H-pyran-4-car

Imidazole lipoxygenase inhibitors

-

, (2008/06/13)

PCT No. PCT/IB96/00744 Sec. 371 Date Jun. 29, 1998 Sec. 102(e) Date Jun. 29, 1998 PCT Filed Jul. 24, 1996 PCT Pub. No. WO97/11079 PCT Pub. Date Mar. 27, 1997The present invention provides a compound of formula (I): and a pharmaceutically acceptable salt thereof, wherein Ar is phenylene optionally substituted with halo, hydroxy, cyano, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 halo-substituted alkyl or C1-C4 halo-substituted alkoxy, X is -A-X1- or -X2-A-, where A is a direct bond or C1-C4 alkylene, and X1 is oxy, thio, sulfinyl or sulfonyl; Ar is phenylene, pyridylene or thienylene optionally substituted with halo, hydroxy, cyano, nitro, amino, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 halo-substituted alkyl, C1-C4 halo-substituted alkoxy, C1-C4 alkylamino or di(C1-C4)alkylamino; Y is CN or CONR1R2 wherein R1 and R2 are independently hydrogen or C1-C4 alkyl; and R is hydrogen or C1-C6 alkyl; W is C2-C3 alkylene, one carbon atom of which may be replaced by an oxygen atom. Further the invention provides a pharmaceutical composition for treating an inflammatory disease, allergy or cardiovascular diseases or the like in a mammalian subject which comprises a compound of formula (I) and a pharmaceutically acceptable carrier.

5-lipoxygenase inhibitors

-

, (2008/06/13)

Novel compounds having the ability to inhibit 5-lipoxygenase enzyme and having the following formula I: STR1 and the pharmaceutically acceptable salts thereof, wherein Ar1 is a heterocyclic moiety which is selected from imidazolyl, pyrrolyl, py

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