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6953-39-5

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6953-39-5 Usage

Description

(5-nitro-1H-indol-3-yl)(oxo)acetic acid is a chemical compound with the molecular formula C10H7N2O6. It is a derivative of indole with a nitro group attached to the 5-position of the indole ring. (5-nitro-1H-indol-3-yl)(oxo)acetic acid also contains an oxoacetic acid moiety. It is used in various research applications, particularly in the synthesis of pharmaceuticals and organic compounds.
Used in Pharmaceutical Industry:
(5-nitro-1H-indol-3-yl)(oxo)acetic acid is used as a building block for the synthesis of pharmaceuticals and organic compounds. Its unique structure and functional groups make it a valuable component in the development of new drugs and therapeutic agents.
Used in Research Applications:
(5-nitro-1H-indol-3-yl)(oxo)acetic acid is used as a reagent in organic synthesis and in the development of new chemical entities with therapeutic potential. Its pharmacological activity has been studied for its anti-cancer and anti-inflammatory properties, making it a promising candidate for further research and development.
Used in Organic Synthesis:
(5-nitro-1H-indol-3-yl)(oxo)acetic acid is used as a reagent in organic synthesis to create a variety of chemical compounds. Its versatile structure and functional groups allow for the formation of new bonds and the synthesis of complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 6953-39-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6953-39:
(6*6)+(5*9)+(4*5)+(3*3)+(2*3)+(1*9)=125
125 % 10 = 5
So 6953-39-5 is a valid CAS Registry Number.

6953-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Nitro-indolyl-3-glyoxylsaeure

1.2 Other means of identification

Product number -
Other names 3-Cyanomethyl-5-nitro-indol

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:6953-39-5 SDS

6953-39-5Relevant articles and documents

An efficient synthesis and biological evaluation of novel analogues of natural product Cephalandole A: A new class of antimicrobial and antiplatelet agents

Sharma, Vashundhra,Jaiswal, Pradeep K.,Kumar, Krishan,Saran, Mukesh,Mathur, Manas,Swami, Ajit K.,Chaudhary, Sandeep

, p. 13 - 19 (2018/06/20)

Cephalandole A 2, a small indole alkaloid isolated from the Taiwanese orchid Cephalanceropsis gracilis (Orchidaceae), exhibits anticancer activity. Surprisingly, this natural product has not been evaluated for any other biological activity so far. To discover other novel potential of Cephalandole A 2, an efficient and economic synthetic protocol for novel Cephalandole A analogues 21a-o has been developed, in only 3 steps from using indole, and applied for their biological activity. Biological testing showed that Cephalandole A 2 and its novel analogues 21a-o exhibited potential antimicrobial and antiplatelet activity in preliminary assay. To the best of our knowledge, this is the first report of Cephalandole A 2 and its novel synthetic analogues 21a-o as a new class of antimicrobial and antiplatelet agents. In this study, 2 and other analogues i.e., 21b, 21d, 21i and 21o showed promising antimicrobial activity against the phytopathogenic bacteria and fungi. Cephalandole A 2, 21c, 21f and 21i, also showed potent antiplatelet activity.

Effect of a hydrogen bonding carboxamide group on universal bases

Too, Kathleen,Brown, Daniel M.,Holliger, Philipp,Loakes, David

, p. 899 - 911 (2008/02/03)

A number of aromatic universal base analogues have been described in the literature, but most are non-hydrogen bonding. We have examined the effect of introducing hydrogen bonding carboxamide groups onto the pyrrole ring of 5-nitroindole. The modified ana

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