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CAS

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147641-94-9

(S)-4-[3-(5-Methyl-2-phenyl-4-oxazolyl)-1-hydroxypropyl]bromobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 147641-94-9 Structure

  • Basic information

    1. Product Name: (S)-4-[3-(5-Methyl-2-phenyl-4-oxazolyl)-1-hydroxypropyl]bromobenzene
    2. Synonyms: (S)-4-[3-(5-Methyl-2-phenyl-4-oxazolyl)-1-hydroxypropyl]bromobenzene
    3. CAS NO:147641-94-9
    4. Molecular Formula:
    5. Molecular Weight: 372.261
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 147641-94-9.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: (S)-4-[3-(5-Methyl-2-phenyl-4-oxazolyl)-1-hydroxypropyl]bromobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-4-[3-(5-Methyl-2-phenyl-4-oxazolyl)-1-hydroxypropyl]bromobenzene(147641-94-9)
    11. EPA Substance Registry System: (S)-4-[3-(5-Methyl-2-phenyl-4-oxazolyl)-1-hydroxypropyl]bromobenzene(147641-94-9)

  • 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: 147641-94-9(Hazardous Substances Data)

147641-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147641-94-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,6,4 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 147641-94:
(8*1)+(7*4)+(6*7)+(5*6)+(4*4)+(3*1)+(2*9)+(1*4)=149
149 % 10 = 9
So 147641-94-9 is a valid CAS Registry Number.

147641-94-9Downstream Products

147641-94-9Relevant articles and documents

Enantioselective Oxazaborolidine Reduction of Ketones Containing Heteroatoms

Quallich, George J.,Woodall, Teresa M.

, p. 785 - 788 (1993)

Ketones which contain heteroatoms, particularly nitrogen, can be enantioselectively and catalytically reduced with chiral oxazaborolidines in the presence of excess borane. Key Words: Enantioselective reduction; Oxazaborolidine; Chiral alcohol; Catalytic reduction; Amine-borane

Hypoglycemic thiazolidinediones and intermediates

-

, (2008/06/13)

Optically pure thiazolidinedione alcohols and ethers, and synthetic intermediates for preparing said alcohols and ethers. These compounds have utility as hypoglycemic and hypocholesterolemic agents.

Process for the preparation of intermediates in the synthesis of chiral thiazolidine-2,4-dione derivatives

-

, (2008/06/13)

A process for the stereoselective preparation of intermediates in the preparation of potent, chiral thiazolidine-2,4-dione hypoglycemics.

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