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4-(4,5-dihydro-3H-pyrrol-2-yl)-phenol is an organic compound with a molecular formula of C11H13NO. It is characterized by a phenol group (C6H5OH) with a 4,5-dihydro-3H-pyrrol-2-yl substituent attached to the para position (4th carbon) of the phenol ring. This pyrrol-2-yl group consists of a pyrrole ring (a five-membered aromatic ring with one nitrogen atom) that is partially saturated, meaning it has one double bond reduced to a single bond. The compound is a white crystalline solid and is used in various chemical and pharmaceutical applications, such as the synthesis of pharmaceuticals and other organic compounds. It is important to note that handling and use of 4-(4,5-dihydro-3H-pyrrol-2-yl)-phenol should be done with proper safety measures due to its potential reactivity and toxicity.

7182-48-1

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7182-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7182-48-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,8 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7182-48:
(6*7)+(5*1)+(4*8)+(3*2)+(2*4)+(1*8)=101
101 % 10 = 1
So 7182-48-1 is a valid CAS Registry Number.

7182-48-1Downstream Products

7182-48-1Relevant academic research and scientific papers

An efficient one-pot synthesis of pyrrolines and tetrahydropyridines from their chloro-precursors via in situ aza-Wittig reaction

Singh, Pradeep N.D.,Klima, Rodney F.,Muthukrishnan, Sivaramakrishnan,Murthy, Rajesh S.,Sankaranarayanan, Jagadis,Stahlecker, Heidi M.,Patel, Bhavika,Gudmundsdóttir, Anna D.

, p. 4213 - 4217 (2005)

A simple and efficient method for synthesizing pyrrolines and tetrahydropyridines via an intramolecular aza-Wittig reaction has been achieved by microwave irradiation of the corresponding chloro-alkane derivatives in the presence of tertiary phosphite and sodium azide. The in situ formation of the alkyl azides makes this a facile and safe method for aza-Wittig reactions.

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