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CAS

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292622-01-6

(2S,3S,4R)-2,3,4-Tris-benzyloxy-2-benzyloxymethyl-cyclopentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 292622-01-6 Structure

  • Basic information

    1. Product Name: (2S,3S,4R)-2,3,4-Tris-benzyloxy-2-benzyloxymethyl-cyclopentanone
    2. Synonyms:
    3. CAS NO:292622-01-6
    4. Molecular Formula:
    5. Molecular Weight: 522.641
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 292622-01-6.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,3S,4R)-2,3,4-Tris-benzyloxy-2-benzyloxymethyl-cyclopentanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3S,4R)-2,3,4-Tris-benzyloxy-2-benzyloxymethyl-cyclopentanone(292622-01-6)
    11. EPA Substance Registry System: (2S,3S,4R)-2,3,4-Tris-benzyloxy-2-benzyloxymethyl-cyclopentanone(292622-01-6)

  • 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: 292622-01-6(Hazardous Substances Data)

292622-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 292622-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,6,2 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 292622-01:
(8*2)+(7*9)+(6*2)+(5*6)+(4*2)+(3*2)+(2*0)+(1*1)=136
136 % 10 = 6
So 292622-01-6 is a valid CAS Registry Number.

292622-01-6Upstream product

292622-01-6Downstream Products

292622-01-6Relevant articles and documents

The polyhydroxy cyclopentene, a total synthesis of (-)-pentenomycin

Seepersaud, Mohindra,Al-Abed, Yousef

, p. 4291 - 4293 (2000)

The functionalized cyclopentene 2 was converted in five steps to (-)- pentenomycin 1. (C) 2000 Elsevier Science Ltd.

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