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CAS

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72402-17-6

(2S,4S)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72402-17-6 Structure

  • Basic information

    1. Product Name: (2S,4S)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran
    2. Synonyms: (2S,4S)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran
    3. CAS NO:72402-17-6
    4. Molecular Formula:
    5. Molecular Weight: 276.292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72402-17-6.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: (2S,4S)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,4S)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran(72402-17-6)
    11. EPA Substance Registry System: (2S,4S)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran(72402-17-6)

  • 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: 72402-17-6(Hazardous Substances Data)

72402-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72402-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,0 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72402-17:
(7*7)+(6*2)+(5*4)+(4*0)+(3*2)+(2*1)+(1*7)=96
96 % 10 = 6
So 72402-17-6 is a valid CAS Registry Number.

72402-17-6Relevant articles and documents

SYNTHESIS OF FOUR STEREOISOMERS OF 4-AMINO-2-(HYDROXY-METHYL)TETRAHYDROFURAN-4-CARBOXYLIC ACID

Yoshimura, Juji,Kondo, Shiro,Ihara, Masaki,Hashimoto, Hironobu

, p. 129 - 142 (2007/10/02)

The 5-benzyl ether, 15, of a 1,2,,4,5-pentanetetrol of known 2S configuration was made by a multistep synthesis from D-ribose.Ring-closure of the 1-O-otosyl derivative, 17, with retention of configuration, followed by oxidation, gave the 2S enantiomer, 22

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