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N-[BIS(METHYLTHIO)METHYLENE]-P-TOLUENESULFONAMIDE is an organic compound that serves as a sulfonamide derivative with potential anticancer and antiparasitic properties. It is utilized as a building block in the synthesis of various biologically active molecules due to its ability to inhibit enzyme activity and its potential anti-inflammatory effects. This chemical is recognized for its diverse pharmacological activities, making it a valuable asset in drug development and research within the field of medicinal chemistry.

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  • 2651-15-2 Structure
  • Basic information

    1. Product Name: N-[BIS(METHYLTHIO)METHYLENE]-P-TOLUENESULFONAMIDE
    2. Synonyms: N-[BIS(METHYLTHIO)METHYLENE]-N-TOSYLAMINE;N-[BIS(METHYLTHIO)METHYLENE]-P-TOLUENESULFONAMIDE;Bismethylthiomethylenetoluenesulfonamide;N-(bis(methylthio)methylene)-P-toluene-sulfonamid;N-(4-Methylphenylsulfonyl)imidodithiocarbonic acid dimethyl ester;N-[bis(methylsulfanyl)methylidene]-4-methylbenzenesulfonamide;N-[bis(methylsulfanyl)methylidene]-4-methyl-benzenesulfonamide;N-[bis(methylthio)methylene]-4-methyl-benzenesulfonamide
    3. CAS NO:2651-15-2
    4. Molecular Formula: C10H13NO2S3
    5. Molecular Weight: 275.41
    6. EINECS: N/A
    7. Product Categories: Sulfur Compounds (for Synthesis);Synthetic Organic Chemistry
    8. Mol File: 2651-15-2.mol
  • Chemical Properties

    1. Melting Point: 109-111 °C(lit.)
    2. Boiling Point: 419°Cat760mmHg
    3. Flash Point: 207.2°C
    4. Appearance: /
    5. Density: 1.27g/cm3
    6. Vapor Pressure: 7.64E-07mmHg at 25°C
    7. Refractive Index: 1.598
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: -6.63±0.50(Predicted)
    11. CAS DataBase Reference: N-[BIS(METHYLTHIO)METHYLENE]-P-TOLUENESULFONAMIDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: N-[BIS(METHYLTHIO)METHYLENE]-P-TOLUENESULFONAMIDE(2651-15-2)
    13. EPA Substance Registry System: N-[BIS(METHYLTHIO)METHYLENE]-P-TOLUENESULFONAMIDE(2651-15-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2651-15-2(Hazardous Substances Data)

2651-15-2 Usage

Uses

Used in Pharmaceutical Industry:
N-[BIS(METHYLTHIO)METHYLENE]-P-TOLUENESULFONAMIDE is used as a precursor in the synthesis of bioactive compounds for its potential anticancer and antiparasitic properties. It is valued for its ability to inhibit enzyme activity, which contributes to its potential therapeutic applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, N-[BIS(METHYLTHIO)METHYLENE]-P-TOLUENESULFONAMIDE is used as a building block for the development of new drugs. Its diverse pharmacological activities make it a promising candidate for further exploration and potential incorporation into novel therapeutic agents.
Used in Drug Development:
N-[BIS(METHYLTHIO)METHYLENE]-P-TOLUENESULFONAMIDE is utilized in drug development for its potential to contribute to the creation of new pharmaceuticals with anti-inflammatory effects. Its role in inhibiting enzyme activity and its potential to be integrated into various biologically active molecules positions it as a key component in the advancement of medicinal treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 2651-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,5 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2651-15:
(6*2)+(5*6)+(4*5)+(3*1)+(2*1)+(1*5)=72
72 % 10 = 2
So 2651-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2S3/c1-8-4-6-9(7-5-8)16(12,13)11-10(14-2)15-3/h4-7H,1-3H3

2651-15-2 Well-known Company Product Price

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  • TCI America

  • (B1389)  N-[Bis(methylthio)methylene]-p-toluenesulfonamide  >95.0%(N)

  • 2651-15-2

  • 5g

  • 490.00CNY

  • Detail

2651-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[bis(methylsulfanyl)methylidene]-4-methylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-<bis(methylthio)methylene>-p-toluenesulfonamide

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:2651-15-2 SDS

2651-15-2Relevant articles and documents

Synthesis of Cyclic Guanidines Bearing N-Arylsulfonyl and N-Cyano Protecting Groups via Pd-Catalyzed Alkene Carboamination Reactions

Peterson, Luke J.,Luo, Jingyi,Wolfe, John P.

supporting information, p. 2817 - 2820 (2017/06/07)

Palladium-catalyzed carboamination reactions of N-allylguanidines bearing cleavable N-cyano or N-arylsulfonyl protecting groups are described. The reactions afford cyclic guanidine products in good yield, and transformations of substrates bearing internal alkenes proceed with high diastereoselectivity. Deuterium labeling studies indicate these transformations proceed via anti-aminopalladation pathways.

Optimization of methods for the generation of carbodiimides for zwitterionic 1,3-diaza-Claisen rearrangements

Walker, Joel D.,Madalengoitia, José S.

supporting information, p. 3786 - 3789 (2015/06/08)

Strained, tertiary, allylic, amine 2-benzyl-2-azabicyclo[2.2.1]hept-5-ene reacts with in situ generated carbodiimides in a 1,3-diaza-Claisen rearrangement to afford structurally interesting bicyclic guanidines. Use of more electron deficient carbodiimides makes these rearrangements more facile; however, there are not sufficient methods for the synthesis of highly electron deficient carbodiimides. Herein reported is the exploration of the synthesis of such carbodiimides from parent ureas and isothioureas and their use in 1,3-diaza-Claisen rearrangements.

Discovery, synthesis,andevaluation of small-molecule signal transducer and activator of transcription 3 inhibitors

Shi, Zhi-Bing,Zhao, Dan,Huang, Yan-Yan,Du, Yun,Cao, Xiang-Rong,Gong, Zhu-Nan,Zhao, Rui,Li, Jian-Xin

, p. 1574 - 1580 (2013/02/23)

The signal transducer and activator of transcription 3 (STAT3) oncogene is a promising molecular target and its inhibitors have great potential as anticancer drugs. To identify novel and STAT3-selective inhibitors, a virtual screening based on Specs and M

Regiospecific synthesis of N-sulfonyl derivatives of 3,5-diamino-1H-1,2,4-triazole and 2,5-diamino-1,3,4-thiadiazole

Maybhate,Rajamohanan,Rajappa

, p. 220 - 222 (2007/10/02)

Condensation of the S,S-dimethyl N-(alkylsulfonyl)carbondithioimidates 1 with aminoguanidine bicarbonate and hydrazinecarbothioamide leads to the regiospecific synthesis of N-sulfonyl derivatives of 3,5-diamino-1H-1,2,4-triazole 2 and 2,5-diamino-1,3,4-thiadiazole 3, respectively.

PYRIDYL GUANIDINE ANTI-ULCER AGENTS

-

, (2008/06/13)

Compounds of the formula STR1 wherein R 1 is a straight or branched chain alkynyl group containing from 3 to 9 carbon atoms, inclusive; R 2 is hydrogen, hydroxy, cyano, (lower)alkyl, (lower) alkoxy, halogen or amino; n is 2 or 3; X is NR 3 or CHR 3 ; R 3

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