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1H-Indol-1-yl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50614-06-7

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50614-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50614-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,1 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50614-06:
(7*5)+(6*0)+(5*6)+(4*1)+(3*4)+(2*0)+(1*6)=87
87 % 10 = 7
So 50614-06-7 is a valid CAS Registry Number.

50614-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name indole radical

1.2 Other means of identification

Product number -
Other names indolyl

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:50614-06-7 SDS

50614-06-7Downstream Products

50614-06-7Relevant academic research and scientific papers

Photoreaction between 2-benzoylthiophene and phenol or indole

Perez-Prieto, Julia,Bosca, Francisco,Galian, Raquel E.,Lahoz, Agustin,Domingo, Luis R.,Miranda, Miguel A.

, p. 5104 - 5113 (2007/10/03)

Laser flash photolysis, density functional theory (DFT) calculations, and product studies have been performed to understand the mechanism of photoreduction of 2-benzoylthiophene (BT) in the presence of phenol or indole. Time-resolved experiments showed th

One-Electron Oxidation of Indoles and Acid-Base Properties of the Indolyl Radicals

Shen, Xinhua,Lind, Johan,Merenyi, Gabor

, p. 4403 - 4406 (2007/10/02)

The rates of attack of OH. N3., Br2.-, CO3.-, and ClO2. on indole and four methylated indoles have been determined.All primary oxidants except for OH. were found to form indolyl radicals quantitatively.The OH. radical produces 44percent indolyl radicals with indole. 3-Methylation affects this yield only slightly while 2- or N-methylation increase the yield of indolyl radicals above 60percent.The acid-base properties of the indolyl radicals have also been explored.Finally the one-electron reduction potential of the radical cation of indole has been determined to be 1.24 +/- 0.01 V.

Photochemical Reactions of Triplet Acetone with Indole, Purine, and Pyrimidine Derivatives

Kasama, Kunihiko,Takematsu, Akiko,Arai, Shigeyoshi

, p. 2420 - 2427 (2007/10/02)

The photochemical reactions of triplet acetone with indole, indole derivatives (1-methyl-, 2-methyl-, 3-methyl-, 5-methyl-, and 7-methylindole, and tryptophan), purine derivatives (caffeine, 7-methylguanine, adenine, adenosine, and guanosine), and a pyrimidine derivative (thymine) have been studied in aqueous solutions by using a KrF or ArF laser.The quenching processes of triplet acetone by indoles, being diffusion controlled, occur via the following paths: triplet-triplet energy transfer, electron transfer, photoaddition of triplet acetone to the 2-carbon atom of the indole ring, and deactivation without a chemical change.The yields of energy transfer, electron transfer, and photoaddition were determined from absorbance measurements.The transient absorptions due to triplet states were observed for caffeine, 7-methylguanine, and thymine, while weak transient absorptions which showed apparent second-order decays were observed for adenine, adenosine, and guanosine.Triplet acetone is quenched mainly via T-T energy transfer in caffeine, 7-methylguanine, and thymine.The weak absorptions may be attributed to neutral radicals in adenine and adenosine and to a cation radical in guanosine.

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