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74209-34-0

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74209-34-0 Usage

Chemical Properties

Yellow Crystals

Uses

Different sources of media describe the Uses of 74209-34-0 differently. You can refer to the following data:
1. A more potent inhibitor of rat cerebellar nitric oxide synthase than 7-nitroindazole
2. Inhibitor of nitric oxide synthase (NOS)
3. 3-Bromo-7-nitroindazole is a potent and selective neuronal nitric oxide synthase (nNOS) inhibitor (1,2). It is also a neuroprotective compound that inhibits the endoplasmic reticulum stress pathway. 3-Bromo-7-nitroindazole has been used to study the role of nitric oxide synthase (nNOS) in spatial memory formation in rats (2).

Check Digit Verification of cas no

The CAS Registry Mumber 74209-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,0 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74209-34:
(7*7)+(6*4)+(5*2)+(4*0)+(3*9)+(2*3)+(1*4)=120
120 % 10 = 0
So 74209-34-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrIN2/c8-7-4-2-1-3-5(9)6(4)10-11-7/h1-3H,(H,10,11)

74209-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-7-nitro-1H-indazole

1.2 Other means of identification

Product number -
Other names 3-bromo-7-nitro-2H-indazole

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:74209-34-0 SDS

74209-34-0Relevant articles and documents

New and efficient synthesis of bi- and trisubstituted indazoles

Bouissane, Latifa,El Kazzouli, Sa?d,Léger, Jean-Michel,Jarry, Christian,Rakib, El Mostapha,Khouili, Mostafa,Guillaumet, Gérald

, p. 8218 - 8225 (2007/10/03)

In this paper, the synthesis of bi- and trisubstituted indazoles was described. 4-Alkoxy-7-aminoprotected-indazole or 7-aminoprotected-indazole derivatives were prepared selectively using SnCl2 in alcohol or SnCl2 in ethyl acetate, r

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