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(2-fluorophenyl)(piperidine-1-yl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69001-07-6 Structure
  • Basic information

    1. Product Name: (2-fluorophenyl)(piperidine-1-yl)methanone
    2. Synonyms: (2-fluorophenyl)(piperidine-1-yl)methanone
    3. CAS NO:69001-07-6
    4. Molecular Formula:
    5. Molecular Weight: 207.248
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69001-07-6.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: (2-fluorophenyl)(piperidine-1-yl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-fluorophenyl)(piperidine-1-yl)methanone(69001-07-6)
    11. EPA Substance Registry System: (2-fluorophenyl)(piperidine-1-yl)methanone(69001-07-6)
  • 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: 69001-07-6(Hazardous Substances Data)

69001-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69001-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,0 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69001-07:
(7*6)+(6*9)+(5*0)+(4*0)+(3*1)+(2*0)+(1*7)=106
106 % 10 = 6
So 69001-07-6 is a valid CAS Registry Number.

69001-07-6Upstream product

69001-07-6Relevant articles and documents

Nitrate-promoted Selective C-H Fluorination of Benzamides and Benzeneacetamides

Ning, Xing-Qian,Lou, Shao-Jie,Mao, Yang-Jie,Xu, Zhen-Yuan,Xu, Dan-Qian

, p. 2445 - 2448 (2018)

A versatile and site-selective nitrate-promoted C-H bond fluorination using various weak coordinating amides as intrinsic directing groups was developed. Diverse tertiary and secondary amides underwent selective aromatic C-H bond fluorination, which featu

METHODS OF CONTROLLING CROP PESTS USING AROMATIC AMIDE INSECT REPELLENTS, METHODS OF MAKING AROMATIC AMIDE INSECT REPELLENTS, AND NOVEL AROMATIC AMIDE INSECT REPELLENTS

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Paragraph 0068-0069, (2022/03/18)

Methods of protecting fruit crops from flying insect pests and of repelling flying insects using aromatic amide compounds are disclosed. The methods apply the compounds to various surfaces, such as the fruit crops, the ground or structures adjacent to the fruit crops, or an object, article, human skin or animal. The compounds have the formula RxC6Hy—C(═O)—N(Cy), where RxC6Hy is a substituted phenyl group, each R group is independently C1-C6 alkyl, substituted C1-C4 alkyl, (substituted) C6-C10 aryl, C1-C4 alkoxy, C6-C10 aryloxy, halogen, nitro, cyano, cyanate, isocyanate, nitroso, C1-C4 alkylthio, phenylthio, (halogen-substituted) C1-C4 alkylsulfonyl, phenylsulfonyl, tolylsulfonyl, amino, mono- or di-C1-C4 alkylamino, diphenylamino, di-C1-C4 alkylamido, formyl, C2-C7 acyl, or C1-C6 alkoxycarbonyl; x is an integer of 1 to 5; x+y=5; Cy is a C2-C8 (substituted) alkadiyl, a C4-C6 (substituted) alkenediyl, or a (substituted) diyl of the formula —(CH2CH2)—O—(CH2CH2)—, —(CH2CH2)—NR′—(CH2CH2)— or —(CH2CH2)—S—(CH2CH2)— that, along with the amide N atom, forms a non-aromatic cyclic group; and R′ is C1-C6 alkyl, substituted C1-C4 alkyl, (substituted) C6-C10 aryl, or (substituted) benzyl.

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