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(2-Methoxy-5-nitrophenyl)acetonitrile is a chemical compound that is commonly used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is a versatile building block in organic chemistry, and its unique structure makes it valuable in various chemical reactions. The presence of a nitro and methoxy group on a benzene ring, along with the acetonitrile functionality, imparts specific properties to the compound, making it useful in the development of a wide range of products.

99459-52-6

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99459-52-6 Usage

Uses

Used in Pharmaceutical Industry:
(2-Methoxy-5-nitrophenyl)acetonitrile is used as an intermediate in the synthesis of various pharmaceutical compounds for its unique structure and properties.
Used in Agrochemical Industry:
(2-Methoxy-5-nitrophenyl)acetonitrile is used as a building block in the development of agrochemicals, contributing to the creation of effective products for agricultural applications.
Used in Organic Chemistry Research:
(2-Methoxy-5-nitrophenyl)acetonitrile is used as a valuable compound in organic chemistry research for its potential in various chemical reactions and its unique structure.
Used in Medicinal Chemistry and Drug Discovery:
(2-Methoxy-5-nitrophenyl)acetonitrile is used as a target for research in medicinal chemistry and drug discovery due to its potential biological activity and its role as an important intermediate in the synthesis of various compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 99459-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,5 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99459-52:
(7*9)+(6*9)+(5*4)+(4*5)+(3*9)+(2*5)+(1*2)=196
196 % 10 = 6
So 99459-52-6 is a valid CAS Registry Number.
InChI:InChI=1S/C9H8N2O3/c1-14-9-3-2-8(11(12)13)6-7(9)4-5-10/h2-3,6H,4H2,1H3

99459-52-6SDS

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 2-(2-methoxy-5-nitrophenyl)acetonitrile

1.2 Other means of identification

Product number -
Other names <2-Methoxy-5-nitro-phenyl>-acetonitril

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:99459-52-6 SDS

99459-52-6Relevant academic research and scientific papers

AMINE-SUBSTITUTED ARYL OR HETEROARYL COMPOUNDS AS EHMT1 AND EHMT2 INHIBITORS

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Paragraph 0561; 0564-0565, (2017/11/10)

The present disclosure relates to amine-substituted aryl or heteroaryl compounds. The present disclosure also relates to pharmaceutical compositions containing these compounds and methods of treating a disorder (e.g., sickle cell anemia) via inhibition of a methyltransferase enzyme selected from EHMT1 and EHMT2, by administering an amine-substituted aryl or heteroaryl compound disclosed herein or a pharmaceutical composition thereof to subjects in need thereof. The present disclosure also relates to the use of such compounds for research or other non-therapeutic purposes.

FUSED AZOLES SUCH AS 2,5-DISUBSTITUTED BENZIMIDAZOLES, BENZOXAZOLES AND BENZOTHIAZOLES AS KINASE INHIBITORS

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Page 125-126, (2008/06/13)

The invention relates to compounds of the formulae (I) to (III) wherein the substituents are as defined in the specification. These compounds have kinase inhibitory activity, such as VEGFR/KDR inhibitory activity. Accordingly, the compounds of the formulae (I) to (III) would be useful in the prevention and treatment of angiogenesis related disorders, ophthalmological conditions, proliferative diseases, inflammatory diseases, and other pathological conditions as described in the specification.

N-phenyl-N-acetamidoglycinamides, their preparation and medicaments containing them

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, (2008/06/13)

Compounds of formula: STR1 in which R1 represents a hydrogen atom or an alkyl, alkoxycarbonyl or an unsubstituted or substituted phenyl radical, R2 represents a hydrogen atom or an unsubstituted or substituted alkyl radical, R3 represents an alkyl, phenylalkyl, indanyl, cycloalkylalkyl or an unsubstituted or substituted phenyl radical, or R2 and R3 form a heterocycle together with the nitrogen atom to which they are attached, and R4 represents an unsubstituted or substituted phenyl radical, a naphthyl, indolyl or quinolyl radical or a phenylamino radical in which the phenyl ring is unsubstituted or substituted, their preparation and medicaments containing them.

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