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887304-94-1

(R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID, also known as (R)-2-hydroxy-2-methyl-4-chlorobenzeneacetic acid, is a derivative of acetic acid with a hydroxy and a methyl group as substituents on the alpha carbon. It is characterized by its pain-relieving and anti-inflammatory properties, which are attributed to its nonsteroidal anti-inflammatory drug (NSAID) classification. The 4-chlorobenzene group in its structure enhances its pharmacological activity, making it a significant compound in medicinal chemistry and drug development.

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  • 887304-94-1 Structure

  • Basic information

    1. Product Name: (R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID
    2. Synonyms: (R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID;(R)-2-(4-Chlorophenyl)-2-hydroxypropionic Acid
    3. CAS NO:887304-94-1
    4. Molecular Formula: C9H9ClO3
    5. Molecular Weight: 200.62
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 887304-94-1.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID(887304-94-1)
    11. EPA Substance Registry System: (R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID(887304-94-1)

  • 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: 887304-94-1(Hazardous Substances Data)

887304-94-1 Usage

Uses

Used in Pharmaceutical Industry:
(R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID is used as a nonsteroidal anti-inflammatory drug (NSAID) for its pain-relieving and anti-inflammatory properties. (R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID's ability to alleviate pain and reduce inflammation makes it a valuable asset in the treatment of various conditions, such as arthritis, headaches, and other inflammatory disorders.
Used in Drug Development:
In the field of drug development, (R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID serves as a key compound due to its chemical structure and properties. Its pharmacological activity, particularly the presence of the 4-chlorobenzene group, makes it a promising candidate for the development of new medications with improved efficacy and reduced side effects.
Used in Medicinal Chemistry Research:
(R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID is utilized in medicinal chemistry research to study the structure-activity relationship of NSAIDs and to design novel compounds with enhanced therapeutic potential. Its unique chemical structure allows researchers to explore various modifications and investigate their impact on the compound's pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 887304-94-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,3,0 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 887304-94:
(8*8)+(7*8)+(6*7)+(5*3)+(4*0)+(3*4)+(2*9)+(1*4)=211
211 % 10 = 1
So 887304-94-1 is a valid CAS Registry Number.

887304-94-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-HYDROXY-2-METHYL(4-CHLOROBENZENE)ACETIC ACID

1.2 Other means of identification

Product number -
Other names (2R)-2-(4-chlorophenyl)-2-hydroxypropanoic acid

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:887304-94-1 SDS

887304-94-1Downstream Products

887304-94-1Relevant articles and documents

Improved practical asymmetric synthesis of α-alkylmandelic acids utilizing highly diastereoselective alkylation of 5-aryl-2-(1-naphthyl)-1,3- dioxolan-4-ones

Misaki, Tomonori,Ureshino, Satoko,Nagase, Ryohei,Oguni, Yumiko,Tanabe, Yoo

, p. 500 - 504 (2012/12/22)

A practical method for the synthesis of optically pure α- alkylmandelic acids 1 is described. The present improved robust method involved two reactions: a mild, convenient, stereo-selective preparation of chiral cis-5-aryl-2-(1-naphthyl)-1,3-dioxolan-4-ones, 9a-c, and highly diastereoselective alkylation of 9a-c, followed by the hydrolysis.

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