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1609101-09-8

C11H14O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1609101-09-8 Structure

  • Basic information

    1. Product Name: C11H14O3
    2. Synonyms: C11H14O3
    3. CAS NO:1609101-09-8
    4. Molecular Formula:
    5. Molecular Weight: 194.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1609101-09-8.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: C11H14O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H14O3(1609101-09-8)
    11. EPA Substance Registry System: C11H14O3(1609101-09-8)

  • 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: 1609101-09-8(Hazardous Substances Data)

1609101-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609101-09-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,1,0 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1609101-09:
(9*1)+(8*6)+(7*0)+(6*9)+(5*1)+(4*0)+(3*1)+(2*0)+(1*9)=128
128 % 10 = 8
So 1609101-09-8 is a valid CAS Registry Number.

1609101-09-8Upstream product

1609101-09-8Downstream Products

1609101-09-8Relevant articles and documents

One-pot organocatalytic enantioselective Michael-Michael-aldol-Henry reaction cascade. A facile entry to the steroid system with six contiguous stereogenic centers

Jhuo, Dai-Huei,Hong, Bor-Cherng,Chang, Chun-Wei,Lee, Gene-Hsiang

, p. 2724 - 2727 (2014)

An expedited method has been developed for the enantioselective synthesis of highly functionalized steroid systems containing six contiguous stereogenic centers with high enantioselectivities (99% ee). The one-pot methodology comprises a cascade of organocatalytic Michael-Michael-aldol-Henry reactions of 7-nitrohept-3-en-2-one and 5-(1-methyl-2,5-dioxocyclopentyl)pent-2-enal. The structure and absolute configuration of the products were confirmed by X-ray analyses of appropriate products.

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