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155694-82-9

2-BROMO-4-METHYLBENZOIC ACID ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 155694-82-9 Structure

  • Basic information

    1. Product Name: 2-BROMO-4-METHYLBENZOIC ACID ETHYL ESTER
    2. Synonyms: 2-BROMO-4-METHYLBENZOIC ACID ETHYL ESTER
    3. CAS NO:155694-82-9
    4. Molecular Formula: C10H11BrO2
    5. Molecular Weight: 243.11
    6. EINECS: N/A
    7. Product Categories: Aromatic Esters
    8. Mol File: 155694-82-9.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.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-BROMO-4-METHYLBENZOIC ACID ETHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-BROMO-4-METHYLBENZOIC ACID ETHYL ESTER(155694-82-9)
    11. EPA Substance Registry System: 2-BROMO-4-METHYLBENZOIC ACID ETHYL ESTER(155694-82-9)

  • 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: 155694-82-9(Hazardous Substances Data)

155694-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155694-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,6,9 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 155694-82:
(8*1)+(7*5)+(6*5)+(5*6)+(4*9)+(3*4)+(2*8)+(1*2)=169
169 % 10 = 9
So 155694-82-9 is a valid CAS Registry Number.

155694-82-9Downstream Products

155694-82-9Relevant articles and documents

2,3-DIHYDROQUINAZOLIN COMPOUNDS AS NAV1.8 INHIBITORS

-

Page/Page column 170; 172, (2021/01/23)

The present invention relates to Nav1.8 Inhibitor 2,3-dihydroquinazolin compounds of Formula (X); wherein Y', X', B', R1', R2', R3', R5', R6', R7', and z1 are as defined herein; or pharmaceutically acceptable salts or tautomer forms thereof, corresponding pharmaceutical compositions or formulations, methods or processes of compound preparation, methods, compounds for use in, uses for and/or combination therapies for treating pain and/or pain-related or associated disease(s), disorder(s) or condition(s), respectively.

Regio- and chemoselective C-H chlorination/bromination of electron-deficient arenes by weak coordination and study of relative directing-group abilities

Sun, Xiuyun,Shan, Gang,Sun, Yonghui,Rao, Yu

supporting information, p. 4440 - 4444 (2013/05/22)

It's all relative: A practical and efficient PdII-catalyzed regio- and chemoselective chlorination/bromination has been developed for the facile synthesis of a broad range of aromatic chlorides. The reaction demonstrates excellent reactivity, good functional-group tolerance, and high yields. A preliminary study was conducted to evaluate relative directing-group abilities of various functionalities. Copyright

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