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225530-14-3

(2S,4EZ)-(+)-tert-butyl 6-benzyloxy-2-N-((1R,2R,5R)-2-hydroxy-3-pinanylidene)imino-3-hexenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 225530-14-3 Structure

  • Basic information

    1. Product Name: (2S,4EZ)-(+)-tert-butyl 6-benzyloxy-2-N-((1R,2R,5R)-2-hydroxy-3-pinanylidene)imino-3-hexenoate
    2. Synonyms:
    3. CAS NO:225530-14-3
    4. Molecular Formula:
    5. Molecular Weight: 441.611
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 225530-14-3.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,4EZ)-(+)-tert-butyl 6-benzyloxy-2-N-((1R,2R,5R)-2-hydroxy-3-pinanylidene)imino-3-hexenoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,4EZ)-(+)-tert-butyl 6-benzyloxy-2-N-((1R,2R,5R)-2-hydroxy-3-pinanylidene)imino-3-hexenoate(225530-14-3)
    11. EPA Substance Registry System: (2S,4EZ)-(+)-tert-butyl 6-benzyloxy-2-N-((1R,2R,5R)-2-hydroxy-3-pinanylidene)imino-3-hexenoate(225530-14-3)

  • 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: 225530-14-3(Hazardous Substances Data)

225530-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 225530-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,5,3 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 225530-14:
(8*2)+(7*2)+(6*5)+(5*5)+(4*3)+(3*0)+(2*1)+(1*4)=103
103 % 10 = 3
So 225530-14-3 is a valid CAS Registry Number.

225530-14-3Relevant articles and documents

An expeditious synthesis of pentosidine, an advanced glycation end product

Yokokawa, Fumiaki,Sugiyama, Hideyuki,Shioiri, Takayuki,Katagiri, Noriko,Oda, Osamu,Ogawa, Hiroshi

, p. 4759 - 4766 (2001)

The chemical synthesis of pentosidine (1), an advanced glycation end product, was achieved via the asymmetric alkylation of the chiral schiff base derived from (+)-2-hydroxy-3-pinanone ((+)-HyPN) and glycine tert-butyl ester, the mercury salt mediated intramolecular guanylation, and the regioselective alkylation of imidazo[4,5-b]pyridine ring. This reliable synthetic achievement will promise availability of pentosidine (1) in quantities.

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