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316152-12-2

2-Thiophenecarboxamide,N-(3,4-dimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 316152-12-2 Structure

  • Basic information

    1. Product Name: 2-Thiophenecarboxamide,N-(3,4-dimethylphenyl)-
    2. Synonyms: 2-Thiophenecarboxamide,N-(3,4-dimethylphenyl)-;N-(3,4-dimethylphenyl)thiophene-2-carboxamide
    3. CAS NO:316152-12-2
    4. Molecular Formula: C13H13NOS
    5. Molecular Weight: 231.31342
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 316152-12-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 289.6±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1 +-.0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 12.66±0.70(Predicted)
    10. CAS DataBase Reference: 2-Thiophenecarboxamide,N-(3,4-dimethylphenyl)-(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Thiophenecarboxamide,N-(3,4-dimethylphenyl)-(316152-12-2)
    12. EPA Substance Registry System: 2-Thiophenecarboxamide,N-(3,4-dimethylphenyl)-(316152-12-2)

  • 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: 316152-12-2(Hazardous Substances Data)

316152-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 316152-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,6,1,5 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 316152-12:
(8*3)+(7*1)+(6*6)+(5*1)+(4*5)+(3*2)+(2*1)+(1*2)=102
102 % 10 = 2
So 316152-12-2 is a valid CAS Registry Number.

316152-12-2Downstream Products

316152-12-2Relevant articles and documents

Para-Selective C-H Amidation of Simple Arenes with Nitriles

Xiang, Shi-Kai,Li, Jin-Mei,Huang, He,Feng, Chun,Ni, Hai-Liang,Chen, Xiao-Zhen,Wang, Bi-Qin,Zhao, Ke-Qing,Hu, Ping,Redshaw, Carl

supporting information, p. 3435 - 3440 (2016/01/25)

A para-selective C-H amidation of simple arenes with nitriles has been developed. By increasing the amount of arenes, a further meta-selective C-H arylation of the produced amides occurred. Both steric and electronic effects are utilized to control the selectivity, resulting in only para-selective amidation products. The readily available nitriles as amidation reagents instead of amides makes the synthesis of N-arylamides more accessible.

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