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Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate is a complex organic chemical compound characterized by the presence of a methyl group, a benzyloxy group, a benzoate group, and a chiral 1R configuration hydroxyethyl group with a bromine atom attached. Its intricate molecular structure, featuring multiple functional groups, suggests a wide range of potential applications in organic synthesis and biochemistry.

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  • 160889-18-9 Structure
  • Basic information

    1. Product Name: Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate
    2. Synonyms:
    3. CAS NO:160889-18-9
    4. Molecular Formula: C17H17BrO4
    5. Molecular Weight: 365.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160889-18-9.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: Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate(160889-18-9)
    11. EPA Substance Registry System: Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate(160889-18-9)
  • 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: 160889-18-9(Hazardous Substances Data)

160889-18-9 Usage

Uses

Used in Organic Synthesis:
Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate is used as a building block in organic synthesis for the creation of more complex molecules. Its diverse functional groups facilitate various chemical reactions, making it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Biochemistry Research:
Due to its unique structure and functional groups, Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate is used in biochemical research to explore its potential interactions with biological systems. It may serve as a probe for understanding enzyme mechanisms, receptor binding, or as a precursor to bioactive molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate is used as a starting material for the development of new drugs. Its structural features may confer specific pharmacological properties, making it a candidate for further optimization and investigation as a potential therapeutic agent.
Used in Chemical Intermediates:
Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate is utilized as a chemical intermediate in the production of various specialty chemicals. Its ability to participate in a range of chemical transformations makes it valuable for the synthesis of dyes, fragrances, and other精细化工 products.

Check Digit Verification of cas no

The CAS Registry Mumber 160889-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,8,8 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 160889-18:
(8*1)+(7*6)+(6*0)+(5*8)+(4*8)+(3*9)+(2*1)+(1*8)=159
159 % 10 = 9
So 160889-18-9 is a valid CAS Registry Number.

160889-18-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]benzoate

1.2 Other means of identification

Product number -
Other names 2-benzyloxy-5-(2-bromo-1(R)-hydroxyethyl)benzoic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:160889-18-9 SDS

160889-18-9Relevant articles and documents

PHENYL SUBSTITUTED PYRAZINOYLGUANIDINE SODIUM CHANNEL BLOCKERS POSSESSING BETA AGONIST ACTIVITY

-

, (2008/06/13)

The present invention relates to sodium channel blockers. The present invention also includes a variety of methods of treatment using these inventive sodium channel blockers.

Enantioselective synthesis of salmeterol via asymmetric borane reduction

Hett, Robert,Stare, Ragnar,Helquist, Paul

, p. 9375 - 9378 (2007/10/02)

Enantioselective syntheses of both enantiomers of salmeterol are accomplished using asymmetric borane reductions with chiral oxazaborolidines as catalysts.

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