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

3289-82-5

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3289-82-5 Usage

Chemical Family

1H-Indole, 1-hydroxybelongs to the indole family of chemical compounds.

Derivative

1H-Indole, 1-hydroxyis a derivative of indole and is commonly found in the human body as a metabolic product of tryptophan, an essential amino acid.

Pharmaceutical Synthesis

1H-Indole, 1-hydroxyis often used as a precursor in the synthesis of various pharmaceutical drugs.

Kidney Function Measurement

1H-Indole, 1-hydroxyis known for its role in the measurement of kidney function through the detection of indoxyl sulfate in urine.

Indigo Dyes

1H-Indole, 1-hydroxyis a key intermediate in the production of indigo dyes.

Organic Synthesis and Chemical Research

1H-Indole, 1-hydroxyhas applications in the field of organic synthesis and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 3289-82-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3289-82:
(6*3)+(5*2)+(4*8)+(3*9)+(2*8)+(1*2)=105
105 % 10 = 5
So 3289-82-5 is a valid CAS Registry Number.

3289-82-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxyindole

1.2 Other means of identification

Product number -
Other names monohydroxyindole

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:3289-82-5 SDS

3289-82-5Relevant academic research and scientific papers

Ultrathin Amorphous/Crystalline Heterophase Rh and Rh Alloy Nanosheets as Tandem Catalysts for Direct Indole Synthesis

Ge, Jingjie,Yin, Peiqun,Chen, Ye,Cheng, Hongfei,Liu, Jiawei,Chen, Bo,Tan, Chaoliang,Yin, Peng-Fei,Zheng, Hong-Xing,Li, Qiang-Qiang,Chen, Shuangming,Xu, Wenjie,Wang, Xiaoqian,Wu, Geng,Sun, Rongbo,Shan, Xiang-Huan,Hong, Xun,Zhang, Hua

, (2021/01/29)

Heterogeneous noble-metal-based catalysis plays an essential role in the production of fine chemicals. Rh-based catalysts are one of the most active candidates for indole synthesis. However, it is still highly desired to develop heterogeneous Rh-based catalysts with high activity and selectivity. In this work, a general, facile wet-chemical method is reported to synthesize ultrathin amorphous/crystalline heterophase Rh and Rh-based bimetallic alloy nanosheets (NSs), including RhCu, RhZn, and RhRu. Impressively, the amorphous/crystalline heterophase Rh NSs exhibit enhanced catalytic activity toward the direct synthesis of indole compared to the crystalline counterpart. Importantly, the obtained amorphous/crystalline heterophase RhCu alloy NSs can further enhance the selectivity to indole of >99.9% and the conversion is 100%. This work demonstrates the importance of phase engineering and metal alloying in the rational design and synthesis of tandem heterogeneous catalysts toward fine chemical synthesis.

Guanine-rich RNAs and DNAs that bind heme robustly catalyze oxygen transfer reactions

Poon, Lester C.-H.,Methot, Stephen P.,Morabi-Pazooki, William,Pio, Frederic,Bennet, Andrew J.,Sen, Dipankar

supporting information; experimental part, p. 1877 - 1884 (2011/04/22)

Diverse guanine-rich RNAs and DNAs that fold to form guanine quadruplexes are known to form tight complexes with Fe(III) heme. We show here that a wide variety of such complexes robustly catalyze two-electron oxidations, transferring oxygen from hydrogen peroxide to thioanisole, indole, and styrene substrates. Use of 18O-labeled hydrogen peroxide reveals the source of the oxygen transferred to form thioanisole sulfoxide and styrene oxide to be the activated ferryl moiety within these systems. Hammett analysis of the kinetics of thioanisole sulfoxide formation is unable to distinguish between a one-step, direct oxygen transfer and a two-step, oxygen rebound mechanism for this catalysis. Oxygen transfer to indole produces a range of products, including indigo and related dyes. Docking of heme onto a high-resolution structure of the G-quadruplex fold of Bcl-2 promoter DNA, which both binds heme and transfers oxygen, suggests a relatively open active site for this class of ribozymes and deoxyribozymes. That heme-dependent catalysis of oxygen transfer is a property of many RNAs and DNAs has ramifications for primordial evolution, enzyme design, cellular oxidative disease, and anticancer therapeutics.

Functionalized heterocycles as modulators of chemokine receptor function and methods of use therefor

-

, (2008/06/13)

Disclosed are novel compounds having the formula or a physiologically acceptable salt, amide, ester or prodrug thereof. The compounds can be used to modulate (antagonize, agonize) chemokine receptor function. Also disclosed is a method for treating a patient having an inflammatory disease and/or viral infection comprising administering an effective amount of a compound of Formula I. In particular embodiments, the invention is a method for treating a patient infected with HIV.

Hypoglycemic imidazoline compounds

-

, (2008/06/13)

This invention relates to certain novel imidazoline compounds and analogues thereof, to their use for the treatment of diabetes, diabetic complications, metabolic disorders, or related diseases where impaired glucose disposal is present, to pharmaceutical compositions comprising them, and to processes for their preparation.

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