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117842-34-9

Oxirane, 2-butyl-3-propyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 117842-34-9 Structure

  • Basic information

    1. Product Name: Oxirane, 2-butyl-3-propyl-
    2. Synonyms: Oxirane, 2-butyl-3-propyl-
    3. CAS NO:117842-34-9
    4. Molecular Formula: C9H18O
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 117842-34-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Oxirane, 2-butyl-3-propyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Oxirane, 2-butyl-3-propyl-(117842-34-9)
    11. EPA Substance Registry System: Oxirane, 2-butyl-3-propyl-(117842-34-9)

  • 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: 117842-34-9(Hazardous Substances Data)

117842-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117842-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,8,4 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 117842-34:
(8*1)+(7*1)+(6*7)+(5*8)+(4*4)+(3*2)+(2*3)+(1*4)=129
129 % 10 = 9
So 117842-34-9 is a valid CAS Registry Number.

117842-34-9Upstream product

117842-34-9Downstream Products

117842-34-9Relevant articles and documents

HIGHLY STEREOSELECTIVE REDUCTION OF β-OXOSULFONIUM SALTS, SYNTHESIS OF trans EPOXIDES

Shimagaki, Masayuki,Matsuzaki, Yuji,Hori, Isaburo,Nakata, Tadashi,Oishi, Takeshi

, p. 4779 - 4782 (2007/10/02)

Alkylation of α-methylthio or α-phenylthio ketones 1 with trimethyloxonium tetrafluoroborate and the reduction of the resulting sulfonium salts 5 with NaBH4 followed by the base treatment afforded trans epoxides 8 with high stereoselectivity.

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