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726180-33-2

Ethanone, 2-hydroxy-1-(2-methoxy-5-methylphenyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 726180-33-2 Structure

  • Basic information

    1. Product Name: Ethanone, 2-hydroxy-1-(2-methoxy-5-methylphenyl)- (9CI)
    2. Synonyms: Ethanone, 2-hydroxy-1-(2-methoxy-5-methylphenyl)- (9CI)
    3. CAS NO:726180-33-2
    4. Molecular Formula: C10H12O3
    5. Molecular Weight: 180.20048
    6. EINECS: N/A
    7. Product Categories: METHOXY
    8. Mol File: 726180-33-2.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: Ethanone, 2-hydroxy-1-(2-methoxy-5-methylphenyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 2-hydroxy-1-(2-methoxy-5-methylphenyl)- (9CI)(726180-33-2)
    11. EPA Substance Registry System: Ethanone, 2-hydroxy-1-(2-methoxy-5-methylphenyl)- (9CI)(726180-33-2)

  • 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: 726180-33-2(Hazardous Substances Data)

726180-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 726180-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,6,1,8 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 726180-33:
(8*7)+(7*2)+(6*6)+(5*1)+(4*8)+(3*0)+(2*3)+(1*3)=152
152 % 10 = 2
So 726180-33-2 is a valid CAS Registry Number.

726180-33-2Upstream product

726180-33-2Relevant articles and documents

Asymmetric hydrogenation of o-alkoxy-substituted arylenamides

Cong-Dung Le, Julie,Pagenkopf, Brian L.

, p. 4177 - 4180 (2007/10/03)

A series of (2-alkoxyaryl)glycinols have been prepared in up to 97.8% ee by asymmetric hydrogenation with cationic rhodium Me-BPE or Me-DuPhos complexes. Others have shown that the presence of ortho substituents on related α-arylenamides causes a decrease in enantioselectivity. However, in this study it was found that o-alkoxy α-arylenamides were reduced with high enantioselectivity irrespective of substituent size.

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