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1446467-05-5

C14H20O6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446467-05-5 Structure

  • Basic information

    1. Product Name: C14H20O6
    2. Synonyms: C14H20O6
    3. CAS NO:1446467-05-5
    4. Molecular Formula:
    5. Molecular Weight: 284.309
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446467-05-5.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: C14H20O6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H20O6(1446467-05-5)
    11. EPA Substance Registry System: C14H20O6(1446467-05-5)

  • 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: 1446467-05-5(Hazardous Substances Data)

1446467-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446467-05-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,4,6 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1446467-05:
(9*1)+(8*4)+(7*4)+(6*6)+(5*4)+(4*6)+(3*7)+(2*0)+(1*5)=175
175 % 10 = 5
So 1446467-05-5 is a valid CAS Registry Number.

1446467-05-5Upstream product

1446467-05-5Relevant articles and documents

Chemo-enzymatic enantioconvergent approach toward ethyl shikimate from ethyl 5-hydroxy-3,4-isopropylidenedioxycyclohex-1-enecarboxylate

Yamashita, Yasunobu,Hanaya, Kengo,Sugai, Takeshi,Mizushima, Tohru,Shoji, Mitsuru

, p. 6527 - 6532 (2013)

An enantioconvergent route for natural form of ethyl shikimate was achieved from Diels-Alder adduct of furan and acryloyl chloride. The key step was a highly enantioselective (E >500) and efficient acetylation of ethyl (3R*,4S*,5S*)-5-hydroxy-3,4-isopropylidenedioxycyclohex-1- enecarboxylate, which had a diastereomeric relationship with ethyl shikimate, mediated by Burkholderia cepacia lipase (Amano PS-IM). Both of the resolved enantiomers were converted to natural form of ethyl shikimate by inversion at C-5 for the former and at C-3 and C-4 for the latter, respectively.

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