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111795-99-4

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111795-99-4 Usage

Description

2-CYANOMETHYL-3-NITRO-6-METHOXY PYRIDINE is a chemical compound with the molecular formula C8H7N3O3. It is a yellow powder that is primarily used as an intermediate in the production of pharmaceuticals and agrochemicals. 2-CYANOMETHYL-3-NITRO-6-METHOXY PYRIDINE is known for its ability to act as a building block in the synthesis of various organic compounds. It is also used in the manufacturing of dyes and as a solvent for organic reactions. Due to its potential health hazards and environmental impact, 2-CYANOMETHYL-3-NITRO-6-METHOXY PYRIDINE is considered to be a hazardous chemical and should be handled with caution.

Uses

Used in Pharmaceutical Industry:
2-CYANOMETHYL-3-NITRO-6-METHOXY PYRIDINE is used as an intermediate in the production of pharmaceuticals for its role in the synthesis of various organic compounds that contribute to the development of new drugs.
Used in Agrochemical Industry:
2-CYANOMETHYL-3-NITRO-6-METHOXY PYRIDINE is used as an intermediate in the production of agrochemicals, where it plays a crucial role in the synthesis of compounds that help in the development of pesticides and other agricultural products.
Used in Dye Manufacturing:
2-CYANOMETHYL-3-NITRO-6-METHOXY PYRIDINE is used in the manufacturing of dyes, where its chemical properties contribute to the creation of various colorants for different applications.
Used as a Solvent in Organic Reactions:
2-CYANOMETHYL-3-NITRO-6-METHOXY PYRIDINE is used as a solvent for organic reactions, facilitating various chemical processes and synthesis in the laboratory and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 111795-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,7,9 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111795-99:
(8*1)+(7*1)+(6*1)+(5*7)+(4*9)+(3*5)+(2*9)+(1*9)=134
134 % 10 = 4
So 111795-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3O3/c1-14-8-3-2-7(11(12)13)6(10-8)4-5-9/h2-3H,4H2,1H3

111795-99-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail
  • Aldrich

  • (701513)  6-Methoxy-3-nitropyridine-2-acetonitrile  97%

  • 111795-99-4

  • 701513-1G

  • 1,109.16CNY

  • Detail
  • Aldrich

  • (701513)  6-Methoxy-3-nitropyridine-2-acetonitrile  97%

  • 111795-99-4

  • 701513-1G

  • 1,109.16CNY

  • Detail
  • Aldrich

  • (701513)  6-Methoxy-3-nitropyridine-2-acetonitrile  97%

  • 111795-99-4

  • 701513-1G

  • 1,109.16CNY

  • Detail
  • Aldrich

  • (701513)  6-Methoxy-3-nitropyridine-2-acetonitrile  97%

  • 111795-99-4

  • 701513-1G

  • 1,109.16CNY

  • Detail

111795-99-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-methoxy-3-nitropyridin-2-yl)acetonitrile

1.2 Other means of identification

Product number -
Other names (6-methoxy-3-nitropyridin-2-yl)acetonitrile

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:111795-99-4 SDS

111795-99-4Relevant articles and documents

Base-mediated reaction of quaternary ammonium salts with nitroarenes - Their useful functionalization via vicarious nucleophilic substitution (VNS)

Jonczyk, Andrzej,Kowalkowska, Anna

, p. 674 - 680 (2002)

Ammonium ylides generated from ammonium salt 1a-e with a base react with derivatives of 3-nitropyridine 2a-c and 2-nitrothiophene (3) to form products of vicarious nucleophilic substitution (VNS) 7, 8, or 9 respectively. The products of VNS 10, 11, or 12 are also produced from the corresponding ammonium salts, a base and 4-chloro-nitrobenzene (4), nitrobenzene (5), or 1-nitronaphthalene (6), respectively. In a few products, an exchange of alkoxy group 7c or substitution of chlorine by alkoxyl 8a,b occured.

3-SUBSTITUTED-1H-PYRROLO[2,3-B]PYRIDINE AND 3-SUBSTITUTED-1H-PYRROLO[3,2-B]PYRIDINE COMPOUNDS, THEIR USE AS MTOR KINASE AND PI3 KINASE INHIBITORS, AND THEIR SYNTHESES

-

Page/Page column 36, (2009/12/23)

The invention relates to 3-substituted-1H-pyrrolo[2,3-b]pyridine, and 3-substituted-1H-pyrrolo[3,2-b]pyridine compounds of the Formula 1: or a pharmaceutically acceptable salt thereof, wherein the constituent variables are as defined herein, compositions comprising the compounds, and methods for making and using the compounds.

Preparation of 4-azaindole and 7-azaindole dimers with a bisalkoxyalkyl spacer in order to preferentially target melatonin MT1 receptors over melatonin MT2 receptors

Larraya, Carlos,Guillard, Jerome,Renard, Pierre,Audinot, Valerie,Boutin, Jean A.,Delagrange, Philippe,Bennejean, Caroline,Viaud-Massuard, Marie-Claude

, p. 515 - 526 (2007/10/03)

Several 4-azaindole and 7-azaindole dimer analogues of melatonin with a bisalkoxyalkyl spacer between the position 5 of each heterocycle were synthetized. Our aim was to investigate the influence of the spacers length on the selectivity of such compounds

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