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5548-10-7

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5548-10-7 Usage

General Description

Indole-3-glyoxylamide is a chemical compound with the molecular formula C11H10N2O2. It is an amide derivative of indole-3-glyoxylic acid, which is a plant growth regulator. Indole-3-glyoxylamide is known to stimulate root formation and promote plant growth. It has been studied for its potential use in agriculture to increase crop yields and improve plant resilience. Its mode of action is thought to be related to its ability to regulate auxin levels in plants, which in turn affects the development and growth of roots. Research on indole-3-glyoxylamide is ongoing to explore its potential in agricultural applications and its impact on plant hormone regulation.

Check Digit Verification of cas no

The CAS Registry Mumber 5548-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,4 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5548-10:
(6*5)+(5*5)+(4*4)+(3*8)+(2*1)+(1*0)=97
97 % 10 = 7
So 5548-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O2/c11-10(14)9(13)7-5-12-8-4-2-1-3-6(7)8/h1-5,12H,(H2,11,14)

5548-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1H-indol-3-yl)-2-oxoacetamide

1.2 Other means of identification

Product number -
Other names Indol-3-yl-glyoxylsaeure-amid

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:5548-10-7 SDS

5548-10-7Relevant articles and documents

Compound containing 2,4 - thiazole ring and preparation method and application thereof

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Paragraph 0189; 0190; 0192, (2021/08/25)

The invention provides a compound containing 2,4 - thiazole rings and a preparation method and application thereof, wherein the compound is shown in a formula X. A Is pyrazolopyrimidine or indole. Z Is carbonless. X Is O or S. Y Is - O - or - NH . R1 Hydrogen or C1 -6 Alkyl. R2 Be selected from C1 - C3 Alkyl. C5 - C15 Alkenyl, alkynyl, 5 - RMB 10 heterocyclic radicals, C6 - C12 Aryl, 5 -12 membered heteroaryl, sterol and 5-10 元 cycloalkyl. Y And R2 Connection, or Y and R2 Looping. R3 From hydrogen. Halogen, amino, hydroxyl, acetyl, 3 - RMB 10 heterocyclic group, C6 - C12 Aryl, 5 -12-membered heteroaryl, 3 -10-membered cycloalkyl, ester, carboxy, trihalomethyl and adamantyl. R2 Or R3 It is unsubstituted or is selected from C. 1 - C6 Alkyl. A hydroxy group, a halogen group, a trihalomethyl group, a carboxyl group, and a phenyl group. R2 Document C1 - C3 Alkyl, R3 Hydrogen.

INDOLE AHR INHIBITORS AND USES THEREOF

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Paragraph 00826; 00828, (2018/11/22)

The present invention provides compounds useful as inhibitors of AHR, compositions thereof, and methods of using the same.

Copper(II)-Mediated Aerobic Oxidation of Benzylimidates: Synthesis of Primary α-Ketoamides

Kumar, Yogesh,Shaw, Mukta,Thakur, Rima,Kumar, Amit

, p. 6617 - 6625 (2016/08/16)

A simple and straightforward method for the synthesis of primary α-ketoamides has been discovered. The reaction represents the first example of benzylimidates directly converting to primary α-ketoamides by using sustainable molecular oxygen as an oxidant. This reaction proceeds in the presence of copper(II) salt via cleavage of benzylic C-H and C-O bonds of the benzylimidates with liberation of alcohols as the only byproduct. A wide substrate scope, operationally mild conditions, the use of single substrates, and a reaction scaled up to grams make this strategy very attractive and practical. Furthermore, mechanistic studies illustrate that the imidate group adjacent to the benzylic position plays crucial role in facilitating this chemical process.

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