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4-(indolizin-2-yl)phenol is an organic compound characterized by a phenol group (C6H4OH) and an indolizin-2-yl moiety. The phenol group consists of a benzene ring with a hydroxyl group attached to the 4th carbon, while the indolizin-2-yl moiety is a heterocyclic ring system derived from indolizine, which is a tricyclic aromatic compound. This chemical structure is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique electronic and steric properties. The compound's specific reactivity, solubility, and stability can be influenced by the presence of the indolizin-2-yl group, making it a subject of interest for chemical research and development.

7496-41-5

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7496-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7496-41-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7496-41:
(6*7)+(5*4)+(4*9)+(3*6)+(2*4)+(1*1)=125
125 % 10 = 5
So 7496-41-5 is a valid CAS Registry Number.

7496-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-indolizin-2-ylphenol

1.2 Other means of identification

Product number -
Other names 2-(4-hydroxyphenyl)indolizine

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:7496-41-5 SDS

7496-41-5Downstream Products

7496-41-5Relevant academic research and scientific papers

Non-imidazole heterocyclic histamine H3 receptor antagonists

Chai, Wenying,Breitenbucher, J. Guy,Kwok, Annette,Li, Xiaobing,Wong, Victoria,Carruthers, Nicholas I.,Lovenberg, Timothy W.,Mazur, Curt,Wilson, Sandy J.,Axe, Frank U.,Jones, Todd K.

, p. 1767 - 1770 (2007/10/03)

Continued exploration of the SAR around the lead imidazopyridine histamine H3 antagonist 1 has led to the discovery of several related series of heterocyclic histamine H3 antagonists. The synthesis and SAR of indolizine, indole and p

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