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2-(4-bromo-2,5-dimethoxyphenyl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 184473-60-7 Structure
  • Basic information

    1. Product Name: 2-(4-bromo-2,5-dimethoxyphenyl)ethanol
    2. Synonyms: 2-(4-bromo-2,5-dimethoxyphenyl)ethanol
    3. CAS NO:184473-60-7
    4. Molecular Formula:
    5. Molecular Weight: 261.115
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 184473-60-7.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: 2-(4-bromo-2,5-dimethoxyphenyl)ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-bromo-2,5-dimethoxyphenyl)ethanol(184473-60-7)
    11. EPA Substance Registry System: 2-(4-bromo-2,5-dimethoxyphenyl)ethanol(184473-60-7)
  • 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: 184473-60-7(Hazardous Substances Data)

184473-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184473-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,4,7 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 184473-60:
(8*1)+(7*8)+(6*4)+(5*4)+(4*7)+(3*3)+(2*6)+(1*0)=157
157 % 10 = 7
So 184473-60-7 is a valid CAS Registry Number.

184473-60-7Relevant articles and documents

Inhibitors of c-Jun N-terminal kinases

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Page/Page column 70, (2008/06/13)

The present invention relates to compounds that are inhibitors of c-jun N-terminal kinase 1, 2, or 3 (JNK1, JNK2, or JNK3), compositions containing the compounds and the use of the compounds in the prevention or treatment of disorders regulated by the activation of JNK1, JNK2 and JNK3.

2-amino-6-(2,4,5-substituted-phenyl)-pyridines

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Page 58, (2010/02/06)

The invention provides compounds of formula VI and the pharmaceutically acceptable salts thereof, wherein R1, R2, R3, and R4 are as defined, to pharmaceutical compositions containing such compounds and to the use of such compounds in the treatment and prevention of central nervous system and other disorders. The invention also provides methods for inhibiting neurological damage caused by impairment of glucose and/or oxygen to the brain in a mammal, which method comprises administering to the mammal a NOS inhibitor. In one embodiment, the NOS inhibitor is administered to the mammal prior to surgery, for example prior to cardiac surgery, angioplasty, or angiography.

NOVEL BENZOPYRAN ANALOGS AND THEIR USE FOR THE TREATMENT OF GLAUCOMA

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Page/Page column 8-9, (2010/02/07)

Novel benzopyran analogs are disclosed. Also disclosed are methods for the lowering and controlling of normal or elevated intraocular pressure as well as a method for the treatment of glaucoma using compositions containing one or more of the compounds of

One-pot Claisen rearrangement/O-methylation/alkene isomerization in the synthesis of ortho-methoxylated phenylisopropylamines

Waldman, Steve R.,Monte, Aaron P.,Bracey, Ann,Nichols, David E.

, p. 7889 - 7892 (2007/10/03)

An improved synthesis of a potent serotonin agonist 1a and its novel derivative 1b is described, making use of a Claisen rearrangement whose unstable phenolic product is methylated and isomerized in situ. This method may be of general use in the synthesis of α-methoxylated phenethylamine derivatives. The synthesis also includes an unusual, one pot demethylation/primary alcohol bromination with boron tribromide.

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