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Benzamide, N,N'-1,7-heptanediylbis[3-chloro-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 27914-34-7 Structure
  • Basic information

    1. Product Name: Benzamide, N,N'-1,7-heptanediylbis[3-chloro-4-methoxy-
    2. Synonyms:
    3. CAS NO:27914-34-7
    4. Molecular Formula: C23H28Cl2N2O4
    5. Molecular Weight: 467.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 27914-34-7.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: Benzamide, N,N'-1,7-heptanediylbis[3-chloro-4-methoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzamide, N,N'-1,7-heptanediylbis[3-chloro-4-methoxy-(27914-34-7)
    11. EPA Substance Registry System: Benzamide, N,N'-1,7-heptanediylbis[3-chloro-4-methoxy-(27914-34-7)
  • 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: 27914-34-7(Hazardous Substances Data)

27914-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27914-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,1 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27914-34:
(7*2)+(6*7)+(5*9)+(4*1)+(3*4)+(2*3)+(1*4)=127
127 % 10 = 7
So 27914-34-7 is a valid CAS Registry Number.

27914-34-7Downstream Products

27914-34-7Relevant articles and documents

N,N'-Heptamethylenebis(4-methoxybenzamide)

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, (2008/06/13)

4-(Q-O)-4'-R1 -N,N'-alkylenebis(benzamides), N,N'-alkylenebis(3,4-methylenedioxybenzamides) or N,N'-alkylenebis[4-(lower-alkoxy)benzamides], having endocrinological properties, where Q is lower-alkyl, lower-alkoxyalkyl, lower-alkenyl, halo-lower-alkyl, halo-lower-alkenyl, lower-cycloalkyl, phenyl and BN-(lower-alkyl) where BN is di-(lower-alkyl)amino or a saturated N-heteromonocyclic radical having from five to seven ring atoms and alkylene has at least five carbon atoms between its two connecting linkages and R1 is Q-O-, hydrogen, lower-alkoxy, lower-alkyl, halo, benzyloxy, hydroxy, di-(lower-alkyl)amino, nitro, amino or trihalomethyl are prepared preferably by reacting the appropriate diamine or N-(aminoalkyl)-benzamide with two or one molar equivalents, respectively, of the appropriate benzoyl halide.

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