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4-(bromomethyl)-N-(tert-butyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 162330-18-9 Structure
  • Basic information

    1. Product Name: 4-(bromomethyl)-N-(tert-butyl)benzamide
    2. Synonyms: 4-(bromomethyl)-N-(tert-butyl)benzamide
    3. CAS NO:162330-18-9
    4. Molecular Formula:
    5. Molecular Weight: 270.169
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 162330-18-9.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: 4-(bromomethyl)-N-(tert-butyl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(bromomethyl)-N-(tert-butyl)benzamide(162330-18-9)
    11. EPA Substance Registry System: 4-(bromomethyl)-N-(tert-butyl)benzamide(162330-18-9)
  • 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: 162330-18-9(Hazardous Substances Data)

162330-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162330-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,3,3 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 162330-18:
(8*1)+(7*6)+(6*2)+(5*3)+(4*3)+(3*0)+(2*1)+(1*8)=99
99 % 10 = 9
So 162330-18-9 is a valid CAS Registry Number.

162330-18-9Relevant articles and documents

2,3-diketone indole compound, preparation method and applications thereof

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Paragraph 0149-0152; 0154, (2020/02/10)

The invention discloses a 2,3-diketone indole compound, a preparation method and applications thereof, wherein the compound has a structure represented by the following general formula (I) or (II). The invention further relates to a pharmaceutical composi

5-methyl-1H-pyrazole derivative, preparation method and applications thereof

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Paragraph 0065-0068, (2018/05/01)

The invention discloses a 5-methyl-1H-pyrazole derivative, a preparation method and applications thereof, wherein the compound has a structure represented by a general formula (I). The invention further provides the preparation method and the applications

Discovery of novel 5-methyl-1H-pyrazole derivatives as potential antiprostate cancer agents: Design, synthesis, molecular modeling, and biological evaluation

Zhang, Daoguang,Asnake, Solomon,Zhang, Jingya,Olsson, Per-Erik,Zhao, Guisen

, p. 1113 - 1124 (2018/03/05)

Androgen receptor (AR) signaling functions as a core driving force for the progression of prostate cancer (PCa), and AR has been proved to be an effective therapeutic target even for castration-resistant prostate cancer (CRPC). Herein, structural modification via a fragments splicing strategy was performed based on two lead compounds T3 and 10e, leading to the discovery of a series of 5-methyl-1H-pyrazole derivatives. AR reporter gene assay revealed compounds A13 and A14 as potent AR antagonists. Some of the compounds in this series inhibited growth of PCa LNCaP cells more efficiently than enzalutamide. A13 and A14 also showed improved metabolic stability compared with 10e in human liver microsomes.

Novel 5α-reductase inhibitors. Synthesis and structure-activity studies of 5-substituted 1-methyl-2-pyridones and 1-methyl-2-piperidones

Hartmann, R. W.,Reichert, M.,Goehring, S.

, p. 807 - 818 (2007/10/02)

In search for nonsteroidal inhibitors of 5α-reductase for the treatment of benign prostatic hyperplasia (BPH) and possibly prostate cancer, substrate mimicks were synthesized comprising of a 1-methyl-2-pyridone (2, 4-16) or 1-methyl-2-piperidone (1, 3, 17

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