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CAS

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178421-64-2

(5S)-3-benzyl-5-hydroxymethyloxazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 178421-64-2 Structure

  • Basic information

    1. Product Name: (5S)-3-benzyl-5-hydroxymethyloxazolidin-2-one
    2. Synonyms: (5S)-3-benzyl-5-hydroxymethyloxazolidin-2-one
    3. CAS NO:178421-64-2
    4. Molecular Formula:
    5. Molecular Weight: 207.229
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 178421-64-2.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: (5S)-3-benzyl-5-hydroxymethyloxazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5S)-3-benzyl-5-hydroxymethyloxazolidin-2-one(178421-64-2)
    11. EPA Substance Registry System: (5S)-3-benzyl-5-hydroxymethyloxazolidin-2-one(178421-64-2)

  • 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: 178421-64-2(Hazardous Substances Data)

178421-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178421-64-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,4,2 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 178421-64:
(8*1)+(7*7)+(6*8)+(5*4)+(4*2)+(3*1)+(2*6)+(1*4)=152
152 % 10 = 2
So 178421-64-2 is a valid CAS Registry Number.

178421-64-2Relevant articles and documents

Synthesis of homochiral tetrahydropteridines

Baker, Stephen J.,Beresford, Kenneth J.M.,Young, Douglas W.

, p. 7221 - 7228 (2017/09/13)

A synthesis of protected homochiral tetrahydropteridines from (2S)-malic acid has been developed. This presents methodology for the synthesis of reduced pteridine coenzymes and pharmaceuticals.

OXAZOLIDINONE DERIVATIVE HAVING INHIBITORY ACTIVITY ON 11 -HYDROXYSTEROID DEHYDROGENASE TYPE I

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Page/Page column 16, (2010/01/29)

Disclosed is a compound which is useful as an 11β-hydroxysteroid dehydrogenase type 1 inhibitor. A compound represented by the formula: , its pharmaceutically acceptable salt, or a solvate thereof, wherein R1 is optionally substituted cycloalky

A straightforward synthesis of L-isoserinal

Junquera, Federico,Merchan, Francisco L.,Merino, Pedro,Tejero, Tomas

, p. 7045 - 7052 (2007/10/03)

A convenient preparation of L-isoserinal 3 in six steps and 32.8% overall yield employing D-glyceraldehyde acetonide I as starting material is described. The procedure is inexpensive, easily scaled up and proceeds without observable racemization.

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