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"2H-Pyrrolium, 3,4-dihydro-1-methyl-5-phenyl, perchlorate" is a complex organic compound with the chemical formula C12H14ClNO2. It is a derivative of pyrrolium, a heterocyclic compound with a five-membered ring containing one nitrogen atom. The 3,4-dihydro-1-methyl-5-phenyl substituents indicate that the compound has a methyl group at the 1-position, a phenyl group at the 5-position, and two hydrogen atoms added to the 3 and 4 positions, making the ring partially saturated. The perchlorate anion (ClO4-) is attached to the cationic pyrrolium, forming an ionic compound. 2H-Pyrrolium, 3,4-dihydro-1-methyl-5-phenyl-, perchlorate is typically used in chemical research and synthesis, and its properties include stability and reactivity, which can be influenced by the presence of the perchlorate anion.

2826-88-2

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2826-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2826-88-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2826-88:
(6*2)+(5*8)+(4*2)+(3*6)+(2*8)+(1*8)=102
102 % 10 = 2
So 2826-88-2 is a valid CAS Registry Number.

2826-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-5-phenyl-3,4-dihydro-2H-pyrrol-1-ium,perchlorate

1.2 Other means of identification

Product number -
Other names 1-methyl-2-phenyl-1-pyrrolinium perchlorate

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:2826-88-2 SDS

2826-88-2Relevant academic research and scientific papers

PHOTOCHEMISTRY OF IMINIUM SALTS. ELECTRON TRANSFER MECHANISMS FOR SINGLET QUENCHING AND PHOTOADDITION OF N-ELECTRON DONATING ALCOHOLS AND ETHERS

Mariano, Patrick S.,Stavinoha, Jerome,Bay, Elliott

, p. 3385 - 3396 (1981)

Several aspects of past and current studies in the area of iminium salt photochemistry are discussed.Investigations of olefin-iminium salt photoaddition and photocyclization reactions are reviewed and conclusions about electron-transfer pathways for fluor

Ring-Chain Tautomerism of Pseudooxynicotine and Some Other Iminium Compounds

Brandaenge, Svante,Lindblom, Lars,Pilotti, Ake,Rodriguez, Benito

, p. 617 - 622 (2007/10/02)

The ring-chain tautomerism in aqueous solution of the nicotine metabolite pseudooxynicotine (1) has been studied.Of the four possible forms of 1, only the chain form 1a and the iminium form 1c could be observed by NMR spectroscopy.The chain form 1a was strongly preponderant at high or low pH.The proportion of 1c reached a maximum level of 52-53 percent in a neutral solution of 1.These results differ strongly from those published by other workers.Some analogous compounds (e.g. 5 and 6) have also been investigated.

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