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1374310-33-4

2,4-dimethyl-6-(phenylethynyl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1374310-33-4 Structure

  • Basic information

    1. Product Name: 2,4-dimethyl-6-(phenylethynyl)aniline
    2. Synonyms: 2,4-dimethyl-6-(phenylethynyl)aniline
    3. CAS NO:1374310-33-4
    4. Molecular Formula:
    5. Molecular Weight: 221.302
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1374310-33-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,4-dimethyl-6-(phenylethynyl)aniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-dimethyl-6-(phenylethynyl)aniline(1374310-33-4)
    11. EPA Substance Registry System: 2,4-dimethyl-6-(phenylethynyl)aniline(1374310-33-4)

  • 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: 1374310-33-4(Hazardous Substances Data)

1374310-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374310-33-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,3,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1374310-33:
(9*1)+(8*3)+(7*7)+(6*4)+(5*3)+(4*1)+(3*0)+(2*3)+(1*3)=134
134 % 10 = 4
So 1374310-33-4 is a valid CAS Registry Number.

1374310-33-4Relevant articles and documents

Base-Promoted Synthesis of Quinoline-4(1H)-thiones from o-Alkynylanilines and Aroyl Isothiocyanates

Modi, Anju,Sau, Prasenjit,Patel, Bhisma K.

, p. 6128 - 6131 (2017)

A base-promoted synthesis of quinoline-4(1H)-thiones has been accomplished from the in situ generated o-alkynylthiourea, obtained by reacting o-alkynylanilines with aroyl/acyl isothiocyanates. A 6-exo-dig S-cyclization of the in situ generated thiourea is

Gold(I)-Catalyzed Reactions between N-(o-Alkynylphenyl)imines and Vinyldiazo Ketones to Form 3-(Furan-2-ylmethyl)-1 H-indoles via Postulated Azallyl Gold and Allylic Cation Intermediates

Kulandai Raj, Antony Sekar,Narode, Akshay Subhash,Liu, Rai-Shung

supporting information, p. 1378 - 1382 (2021/03/03)

This work describes gold-catalyzed additions of vinyldiazo ketones to N-(o-alkynylphenyl)imines to yield 3-(furan-2-ylmethyl)-1H-indoles involving skeletal rearrangement; these new catalytic reactions are applicable to a wide range of substrates. We postu

An expedient route to tricyanovinylindoles and indolylmaleimides fromo-alkynylanilines utilising DMSO as a one-carbon synthon

Chakraborty, Nikita,Dahiya, Anjali,Modi, Anju,Patel, Bhisma K.,Rakshit, Amitava

, p. 6847 - 6857 (2021/08/20)

A Pd(ii)/Cu(ii) catalysed domino synthesis of tricyanovinylindoles has been achieved using DMSO as a one-carbon synthon. The reaction proceedsviathe construction of 2-aryl-3-formyl indole followed by sequential addition of malononitrile and a CN resulting

Synthesis of bis-exocyclic conjugated diene containing 1,2,3,4-tetrahydroquinoline derivatives via palladium-catalyzed intramolecular Heck cyclization

Ghosh, Munmun,Dhara, Shubhendu,Nuree, Yasin,Ray, Jayanta K.

, p. 41561 - 41564 (2014/12/10)

An efficient method has been developed for the synthesis of bis-exocyclic conjugated diene containing 1,2,3,4-tetrahydroquinoline derivatives via palladium-catalyzed intramolecular Heck cyclization of (2-bromo-allyl)-(2-phenylethynyl-phenyl)-amines. The r

Synthesis of bis-exocyclic conjugated diene containing 1,2,3,4-tetrahydroquinoline derivatives via palladium-catalyzed intramolecular Heck cyclization

Ghosh, Munmun,Dhara, Shubhendu,Nuree, Yasin,Ray, Jayanta K.

, p. 41561 - 41564 (2015/05/20)

An efficient method has been developed for the synthesis of bis-exocyclic conjugated diene containing 1,2,3,4-tetrahydroquinoline derivatives via palladium-catalyzed intramolecular Heck cyclization of (2-bromo-allyl)-(2-phenylethynyl-phenyl)-amines. The r

Protonated DBU as catalyst for cascade addition-cyclization of 2-alkynylaniline and carbon disulfide

Zhao, Peng,Liao, Qian,Gao, Hongxin,Xi, Chanjuan

supporting information, p. 2357 - 2361 (2013/06/26)

Protonated 1,8-diazabicyclo[5,4,0]undec-7-ene as catalyst for cascade addition/cyclization of 2-alkynylaniline and carbon disulfide has been described. This process provides a convenient route for synthesis of a variety of benzo[d][1,3]thiazine-2(4H)-thio

Palladium-catalyzed intermolecular aerobic oxidative cyclization of 2-ethynylanilines with isocyanides: Regioselective synthesis of 4-halo-2-aminoquinolines

Liu, Bifu,Gao, Hanling,Yu, Yue,Wu, Wanqing,Jiang, Huanfeng

supporting information, p. 10319 - 10328 (2013/11/06)

A robust and regioselective palladium-catalyzed intermolecular aerobic oxidative cyclization of 2-ethynylanilines with isocyanides to the synthesis of 4-halo-2-aminoquinolines is reported herein. The procedure constructs various 4-halo-2-aminoquinolines w

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