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117067-50-2

N-(1-Benzotriazol-1-yl-nonyl)-benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 117067-50-2 Structure

  • Basic information

    1. Product Name: N-(1-Benzotriazol-1-yl-nonyl)-benzamide
    2. Synonyms: N-(1-Benzotriazol-1-yl-nonyl)-benzamide
    3. CAS NO:117067-50-2
    4. Molecular Formula:
    5. Molecular Weight: 364.491
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 117067-50-2.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: N-(1-Benzotriazol-1-yl-nonyl)-benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1-Benzotriazol-1-yl-nonyl)-benzamide(117067-50-2)
    11. EPA Substance Registry System: N-(1-Benzotriazol-1-yl-nonyl)-benzamide(117067-50-2)

  • 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: 117067-50-2(Hazardous Substances Data)

117067-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117067-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,0,6 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117067-50:
(8*1)+(7*1)+(6*7)+(5*0)+(4*6)+(3*7)+(2*5)+(1*0)=112
112 % 10 = 2
So 117067-50-2 is a valid CAS Registry Number.

117067-50-2Relevant articles and documents

THE CHEMISTRY OF BENZOTRIAZOLE. PART 8. A NOVEL TWO-STEP PROCEDURE FOR THE N-ALKYLATION OF AMIDES

Katritzky, Alan R.,Drewniak, Malgorzata

, p. 2339 - 2344 (2007/10/02)

Benzotriazole, aldehydes RCHO, and amides R1CONH2 react together with elimination of water to form 1:1:1 adducts which are reduced smoothly by NaBH4 to give the N-substituted amides R1CONHCH2R.Both steps occur in high yields and can be carried out on a large scale, thus comprising a convenient general method for the N-alkylation of amides.

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