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CAS

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944401-59-6

(+)-4-epi-valienamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 944401-59-6 Structure

  • Basic information

    1. Product Name: (+)-4-epi-valienamine
    2. Synonyms:
    3. CAS NO:944401-59-6
    4. Molecular Formula:
    5. Molecular Weight: 175.185
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 944401-59-6.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: (+)-4-epi-valienamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+)-4-epi-valienamine(944401-59-6)
    11. EPA Substance Registry System: (+)-4-epi-valienamine(944401-59-6)

  • 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: 944401-59-6(Hazardous Substances Data)

944401-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 944401-59-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,4,0 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 944401-59:
(8*9)+(7*4)+(6*4)+(5*4)+(4*0)+(3*1)+(2*5)+(1*9)=166
166 % 10 = 6
So 944401-59-6 is a valid CAS Registry Number.

944401-59-6Upstream product

944401-59-6Downstream Products

944401-59-6Relevant articles and documents

Stereoselective total synthesis of (+)-valienamine and (+)-4-epi- valienamine via a ring-closing enyne metathesis protocol

Radha Krishna, Palakodety,Srinivas Reddy

, p. 209 - 212 (2009)

Stereoselective total synthesis of (+)-valienamine is reported utilizing Sharpless asymmetric dihydroxylation, diastereoselective Carreira alkynylation, and ring-closing enyne metathesis (RCEYM) as key steps from L-serine. A similar strategy is also reported for the first total synthesis of (+)-4-epi- valienamine. Georg Thieme Verlag Stuttgart.

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