Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2-(methylamino)benzonitrile, also known as N-methyl-2-aminobenzonitrile, is a chemical compound characterized by the molecular formula C8H8N2. It presents as a white to pale yellow solid and is categorized under aromatic amines. 2-(methylamino)benzonitrile is utilized in various chemical processes due to its reactivity and structural properties.

17583-40-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 17583-40-3 Structure
  • Basic information

    1. Product Name: 2-(methylamino)benzonitrile
    2. Synonyms: 2-(methylamino)benzonitrile;Benzonitrile,2-(methylamino)-
    3. CAS NO:17583-40-3
    4. Molecular Formula: C8H8N2
    5. Molecular Weight: 132
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17583-40-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 277.6 °C at 760 mmHg
    3. Flash Point: 121.7°C
    4. Appearance: /
    5. Density: 1.06 g/cm3
    6. Vapor Pressure: 0.00448mmHg at 25°C
    7. Refractive Index: 1.551
    8. Storage Temp.: 2-8°C(protect from light)
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(methylamino)benzonitrile(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(methylamino)benzonitrile(17583-40-3)
    12. EPA Substance Registry System: 2-(methylamino)benzonitrile(17583-40-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 17583-40-3(Hazardous Substances Data)

17583-40-3 Usage

Uses

Used in Pharmaceutical Industry:
2-(methylamino)benzonitrile is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and medicinal compounds. Its unique structure allows it to be a key intermediate in the creation of various pharmaceutical agents.
Used in Dye Industry:
In the dye industry, 2-(methylamino)benzonitrile is employed as a precursor in the production of dyes. Its aromatic amine nature facilitates the synthesis of a range of colorants used in different applications, including textiles, plastics, and printing inks.
Used in Organic Synthesis:
2-(methylamino)benzonitrile is utilized as an intermediate in organic synthesis, playing a crucial role in the formation of a variety of organic compounds. Its versatility in chemical reactions makes it a valuable component in the synthesis of specialty chemicals and other complex organic molecules.
Safety Note:
It is important to handle 2-(methylamino)benzonitrile with care, as it may pose health risks if inhaled, swallowed, or absorbed through the skin. Proper safety measures should be taken to minimize exposure and ensure the safe use of this compound in industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 17583-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,8 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17583-40:
(7*1)+(6*7)+(5*5)+(4*8)+(3*3)+(2*4)+(1*0)=123
123 % 10 = 3
So 17583-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2/c1-10-8-5-3-2-4-7(8)6-9/h2-5,10H,1H3

17583-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methylamino)benzonitrile

1.2 Other means of identification

Product number -
Other names N-methylanthranilonitrile

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:17583-40-3 SDS

17583-40-3Relevant articles and documents

Nickel/Photo-Cocatalyzed Asymmetric Acyl-Carbamoylation of Alkenes

Fan, Pei,Lan, Yun,Zhang, Chang,Wang, Chuan

supporting information, p. 2180 - 2186 (2020/03/03)

An unprecedented asymmetric acyl-carbamoylation of pendant alkenes tethered on aryl carbamic chlorides with both aliphatic and aromatic aldehydes has been developed via the cooperative catalysis of a chiral nickel-PHOX complex and tetrabutylammonium decatungstate. This reaction represents the first example of merging hydrogen-atom-transfer photochemistry and asymmetric transition metal catalysis in difunctionalization of alkenes. Using this protocol, a variety of oxindoles bearing a challenging quaternary stereogenic center are furnished under mild conditions in highly enantioselective manner.

One-Pot Synthesis of 4-Quinolone via Iron-Catalyzed Oxidative Coupling of Alcohol and Methyl Arene

Lee, Seok Beom,Jang, Yoonkyung,Ahn, Jiwon,Chun, Simin,Oh, Dong-Chan,Hong, Suckchang

supporting information, p. 8382 - 8386 (2020/11/18)

Herein, we describe the iron(III)-catalyzed oxidative coupling of alcohol/methyl arene with 2-amino phenyl ketone to synthesize 4-quinolone. Alcohols and methyl arenes are oxidized to the aldehyde in the presence of an iron catalyst and di-tert-butyl peroxide, followed by a tandem process, condensation with amine/Mannich-type cyclization/oxidation, to complete the 4-quinolone ring. This method tolerates various kinds of functional groups and provides a direct approach to the synthesis of 4-quinolones from less functionalized substrates.

Selective N-monomethylation of primary anilines with dimethyl carbonate in continuous flow

Seo, Hyowon,Bédard, Anne-Catherine,Chen, Willie P.,Hicklin, Robert W.,Alabugin, Alexander,Jamison, Timothy F.

, p. 3124 - 3128 (2017/12/11)

Selective N-monomethylation of anilines has been achieved under continuous flow conditions using dimethyl carbonate as a green methylating agent in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene. Our methodology takes advantage of the expanded process windows available in the continuous flow regime to safely induce monomethylation in superheated solvents at high pressure. We propose selective N-monomethylation is achieved via an in situ protection-deprotection pathway, which is supported by the observed reactivities of several putative reaction intermediates. The robust and scalable method was applicable to a broad range of primary aniline substrates including ortho-, meta-, and para-substituted anilines, as well as electron-rich and electron-deficient anilines. The synthetic precursor of diazepam, 5-chloro-2-(methylamino)benzophenone, was selectively synthesized under our optimized conditions.

A Synthesis of 1H-Indazoles via a Cu(OAc)2-Catalyzed N-N Bond Formation

Chen, Cheng-Yi,Tang, Guangrong,He, Fengxian,Wang, Zhaobin,Jing, Hailin,Faessler, Roger

supporting information, p. 1690 - 1693 (2016/04/26)

A facile synthesis of 1H-indazoles featuring a Cu(OAc)2-catalyzed N-N bond formation using oxygen as the terminal oxidant is described. The reaction of readily available 2-aminobenzonitriles with various organometallic reagents led to o-aminoar

Rhodium(III)-Catalyzed Direct Cyanation of Aromatic C-H Bond to Form 2-(Alkylamino)benzonitriles Using N-Nitroso As Directing Group

Dong, Jiawei,Wu, Zhongjie,Liu, Zhengyi,Liu, Ping,Sun, Peipei

, p. 12588 - 12593 (2016/01/09)

2-(Alkylamino)benzonitriles were synthesized via a rhodium-catalyzed cyanation on the aryl C-H bond and subsequent denitrosation of N-nitrosoarylamines using a removable nitroso as the directing group, in which N-cyano-N-phenyl-p-methylbenzenesulfonamide (NCTS) was used as the "CN" source. Various substituents on the aryl ring and amino group of N-nitrosoarylamines tolerated the reaction, and the corresponding products were achieved in moderate to good yields.

Copper(II)-catalyzed oxidative N-nitrosation of secondary and tertiary amines with nitromethane under an oxygen atmosphere

Sakai, Norio,Sasaki, Minoru,Ogiwara, Yohei

supporting information, p. 11638 - 11641 (2015/07/15)

The combination of a catalytic amount of Cu(OTf)2 and less than a stoichiometric amount of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) under an O2 atmosphere effectively promoted the N-nitrosation of both secondary aromatic/aliphatic amines and tertiary aromatic amines with nitromethane (CH3NO2) leading to the preparation of N-nitrosamine derivatives.

Alkali-metal mediated zincation of N-heterocyclic substrates using the lithium zincate complex, (THF)Li(TMP)Zn(tBu)2 and applications in in situ cross coupling reactions

Blair, Victoria L.,Blakemore, David C.,Hay, Duncan,Hevia, Eva,Pryde, David C.

scheme or table, p. 4590 - 4594 (2011/09/30)

This study investigates the ability of the mixed-metal reagent [Li(TMP)Zn(tBu)2] 1 to promote direct Zn-H exchange reactions (zincations) of a wide range of N-heterocyclic molecules. The generated metallated intermediates from these reactions are intercepted with I2 and some of them are also employed as precursors in Pd-catalysed Negishi cross-coupling applications. A comparison with recent precedents in metallation chemistry reveals that for some of these heterocycles, 1 allows improved conversions, under milder conditions and in certain cases, even gives unique regioselectivities.

Selective monomethylation of anilines by Cu(OAc)2-promoted cross-coupling with MeB(OH)2

Gonzalez, Israel,Mosquera, Jesus,Guerrero, Cesar,Rodriguez, Ramon,Cruces, Jacobo

supporting information; experimental part, p. 1677 - 1680 (2009/09/06)

N-Methylanilines are readily synthesized in high yields through the copper(ll)-promoted coupling of anilines and methylboronic acid. This method represents a new approach for the selective monomethylation of anilines, and it is the first reported example

2-Arylaminopyrimidine derivatives as PLK inhibitors

-

Page/Page column 43, (2010/02/14)

Anilino-pyrimidine and 1,2,4-triazine compounds (1) are new. Anilino-pyrimidine and 1,2,4-triazine compounds of formula (1), their tautomers, racemates, enantiomers and/or diastereomers and acid-addition salts are new. X : NR 1a>, O or S; Y : CH or N; Z : hydrogen, halo, (halo)1-3C alkyl, 2-3C alkenyl, 2-3C alkynyl, formyl, 1-3C (halo)alkylcarbonyl, 2-3C alkenyl-, 2-3C alkynyl-carbonyl or pseudohalo; A : (hetero)aryl group (i) or (ii); R a> - R f>e.g. hydrogen, halo or nitro; R 1> and R 1a>hydrogen or methyl; R 2>e.g. Cl, Br, I, OR 6>; R 3>e.g. -CONR 1>-L-Q 3-Q 4-R 9>, -NR 1>-CO-L-Q 3-Q 4-R 9>; R 4>e.g. OR 6>, COR 6>, CONR 6>R 7>, NR 6>R 7>, NR 6>COR 7>, NR 6>SO 2R 7>, N=CR 6>R 7>, SR 6>, SOR 6>, SO 2R 6>, SO 2NR 6>R 7> or pseudohalogen, or any of 1-8C alkyl, 2-10C alkenyl or alkynyl, 3-8C cycloalkyl, (hetero)aryl or heterocyclyl; R 5>hydrogen, halo, trifluoromethyl, 1-3C alkyl or OR 6>; R 6>, R 7>e.g. hydrogen or any of 1-5C alkyl, 2-5C alkenyl or alkynyl, 3-10C cycloalkyl, (hetero)aryl or heterocyclyl; L : e.g. bond or residue of 1-16C alkyl, 2-16C alkenyl or alkynyl, 3-10C cycloalkyl, (hetero)aryl or heterocyclyl; Q 3 and Q 4bond or a mono- or bi-cyclic heterocyclyl, optionally substituted by one or more of Me, Et, halo, amino, hydroxy or pseudohalo; R 9>as L but not a bond; and T : N, O or S. Full definitions are given in the DEFINITIONS (Full Definitions) field. [Image] [Image] ACTIVITY : Cytostatic; Antiinflammatory; Immunosuppressive; Virucide; Anti-HIV; Dermatological; Nootropic; Neuroprotective; Nephrotropic; Vulnerary; Antibacterial; Fungicide; Antiparasitic; Antipsoriatic; Osteopathic; Cardiovascular-Gen; Vasotropic; Gastrointestinal-Gen. MECHANISM OF ACTION : Kinase inhibitor; Polo-like kinase (PLK) inhibitor. In a trial, (1) was found to have EC 50 against recombinant human PLK1 of below 5, generally 1 mu M. No results for specific compounds were given.

Synthesis and β-glucuronidase mediated cleavage of an alcohol prodrug incorporating a double spacer moiety

Papot,Rivault,Tranoy,Gesson

, p. 164 - 166 (2007/10/03)

An alcohol prodrug has been prepared by incorporation of two spacer groups between the trigger (glucuronic acid) and nitroveratryl alcohol, used as a model. Release of the later has been observed after hydrolysis of the glycoside by β-glucuronidase. Such prodrugs may find application in ADEPT or PMT potocols in cancer chemotherapy.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 17583-40-3