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115890-32-9

(2R,3R)-2-azido-1-(benzyloxy)-3,4-epoxybutane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115890-32-9 Structure

  • Basic information

    1. Product Name: (2R,3R)-2-azido-1-(benzyloxy)-3,4-epoxybutane
    2. Synonyms: (2R,3R)-2-azido-1-(benzyloxy)-3,4-epoxybutane
    3. CAS NO:115890-32-9
    4. Molecular Formula:
    5. Molecular Weight: 219.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115890-32-9.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: (2R,3R)-2-azido-1-(benzyloxy)-3,4-epoxybutane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R)-2-azido-1-(benzyloxy)-3,4-epoxybutane(115890-32-9)
    11. EPA Substance Registry System: (2R,3R)-2-azido-1-(benzyloxy)-3,4-epoxybutane(115890-32-9)

  • 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: 115890-32-9(Hazardous Substances Data)

115890-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115890-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,8,9 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115890-32:
(8*1)+(7*1)+(6*5)+(5*8)+(4*9)+(3*0)+(2*3)+(1*2)=129
129 % 10 = 9
So 115890-32-9 is a valid CAS Registry Number.

115890-32-9Relevant articles and documents

Enantioselective synthesis of (-)-kainic acid

Takano,Sugihara,Satoh,Ogasawara

, p. 6467 - 6471 (1988)

Novel diastereoselectivity in the intramolecular Diels-Alder reaction of the heterodiene 18 has been observed. The structure of the cycloadduct was determined to be 20, possessing cis-5/6 ring juncture by converting it into (-)-kainic acid and kainic acid lactone.

Synthesis of the 1,4-diazepan-2-one moiety of liposidomycins

Kim, Kwan Soo,Cho, In Haeng,Ahn, Yeong Hee,Park, Jong Ii

, p. 1783 - 1786 (2007/10/02)

The two stereoisomers 12 and 16 of 1,4-dimethyl-1,4-diazepan-2-one, a central feature of liposidomycins, have been synthesized starting from L-ascorbic acid and sarcosine.

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