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331270-15-6

4-methyl-N-(5,6,7,8-tetrahydronaphthalen-1-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 331270-15-6 Structure

  • Basic information

    1. Product Name: 4-methyl-N-(5,6,7,8-tetrahydronaphthalen-1-yl)benzamide
    2. Synonyms: 4-methyl-N-(5,6,7,8-tetrahydronaphthalen-1-yl)benzamide
    3. CAS NO:331270-15-6
    4. Molecular Formula: C18H19NO
    5. Molecular Weight: 265.34956
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 331270-15-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-methyl-N-(5,6,7,8-tetrahydronaphthalen-1-yl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methyl-N-(5,6,7,8-tetrahydronaphthalen-1-yl)benzamide(331270-15-6)
    11. EPA Substance Registry System: 4-methyl-N-(5,6,7,8-tetrahydronaphthalen-1-yl)benzamide(331270-15-6)

  • 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: 331270-15-6(Hazardous Substances Data)

331270-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 331270-15-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,2,7 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 331270-15:
(8*3)+(7*3)+(6*1)+(5*2)+(4*7)+(3*0)+(2*1)+(1*5)=96
96 % 10 = 6
So 331270-15-6 is a valid CAS Registry Number.

331270-15-6Downstream Products

331270-15-6Relevant articles and documents

Carbon-Carbon Bond Formation of Trifluoroacetyl Amides with Grignard Reagents via C(O)-CF3 Bond Cleavage

Zhu, Longzhi,Le, Liyuan,Yan, Mingpan,Au, Chak-Tong,Qiu, Renhua,Kambe, Nobuaki

, (2019/05/07)

The reaction of trifluoroacetyl amides with Grignard reagent for the substitution of CF3 group with various alkyl or aryl groups is described. A variety of aryl, quinolin-8-yl, and (hetero)alkyl functional groups as well as F, Cl, and Br atoms are well tolerated. These moisture-stable and easily available trifluoroacetyl amides can be conveniently obtained and used as new versatile precursors for isocyanates. The control experiments show that the reaction proceeds via an isocyanate intermediate and/or alkoxide/amide dual anionic intermediate.

Carbon-Carbon Bond Formation of Trifluoroacetyl Amides with Grignard Reagents via C(O)-CF3 Bond Cleavage

Zhu, Longzhi,Le, Liyuan,Yan, Mingpan,Au, Chak-Tong,Qiu, Renhua,Kambe, Nobuaki

, p. 5635 - 5644 (2019/05/10)

The reaction of trifluoroacetyl amides with Grignard reagent for the substitution of CF3 group with various alkyl or aryl groups is described. A variety of aryl, quinolin-8-yl, and (hetero)alkyl functional groups as well as F, Cl, and Br atoms are well tolerated. These moisture-stable and easily available trifluoroacetyl amides can be conveniently obtained and used as new versatile precursors for isocyanates. The control experiments show that the reaction proceeds via an isocyanate intermediate and/or alkoxide/amide dual anionic intermediate.

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