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314765-45-2

N-heptyl-2-methylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 314765-45-2 Structure

  • Basic information

    1. Product Name: N-heptyl-2-methylbenzamide
    2. Synonyms: N-heptyl-2-methylbenzamide
    3. CAS NO:314765-45-2
    4. Molecular Formula: C15H23NO
    5. Molecular Weight: 233.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 314765-45-2.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: N-heptyl-2-methylbenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-heptyl-2-methylbenzamide(314765-45-2)
    11. EPA Substance Registry System: N-heptyl-2-methylbenzamide(314765-45-2)

  • 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: 314765-45-2(Hazardous Substances Data)

314765-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 314765-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,4,7,6 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 314765-45:
(8*3)+(7*1)+(6*4)+(5*7)+(4*6)+(3*5)+(2*4)+(1*5)=142
142 % 10 = 2
So 314765-45-2 is a valid CAS Registry Number.

314765-45-2Downstream Products

314765-45-2Relevant articles and documents

One-pot synthesis of amides from aldehydes and amines via C-H bond activation

Cadoni, Roberta,Porcheddu, Andrea,Giacomelli, Giampaolo,De Luca, Lidia

supporting information, p. 5014 - 5017,4 (2012/12/12)

A one-pot synthesis of amides from aldheydes with N-chloroamines, prepared in situ from amines, has been developed. Both aliphatic and aromatic aldehydes and many types of mono- and disubstituted amines are tolerant in this transformation. This cross-coupling reaction appears simple and convenient, has a wide substrate scope and makes use of cheap, abundant, and easily available reagents.

One-pot synthesis of amides from aldehydes and amines via C-H bond activation

Cadoni, Roberta,Porcheddu, Andrea,Giacomelli, Giampaolo,De Luca, Lidia

supporting information, p. 5014 - 5017 (2013/01/15)

A one-pot synthesis of amides from aldheydes with N-chloroamines, prepared in situ from amines, has been developed. Both aliphatic and aromatic aldehydes and many types of mono- and disubstituted amines are tolerant in this transformation. This cross-coupling reaction appears simple and convenient, has a wide substrate scope and makes use of cheap, abundant, and easily available reagents.

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