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5-Hexen-1-one, 1-(2,4-dihydroxyphenyl)-2-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 526208-47-9 Structure
  • Basic information

    1. Product Name: 5-Hexen-1-one, 1-(2,4-dihydroxyphenyl)-2-methyl- (9CI)
    2. Synonyms: 5-Hexen-1-one, 1-(2,4-dihydroxyphenyl)-2-methyl- (9CI)
    3. CAS NO:526208-47-9
    4. Molecular Formula: C13H16O3
    5. Molecular Weight: 220.26434
    6. EINECS: N/A
    7. Product Categories: ALCOHOL
    8. Mol File: 526208-47-9.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: 5-Hexen-1-one, 1-(2,4-dihydroxyphenyl)-2-methyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Hexen-1-one, 1-(2,4-dihydroxyphenyl)-2-methyl- (9CI)(526208-47-9)
    11. EPA Substance Registry System: 5-Hexen-1-one, 1-(2,4-dihydroxyphenyl)-2-methyl- (9CI)(526208-47-9)
  • 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: 526208-47-9(Hazardous Substances Data)

526208-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 526208-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,6,2,0 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 526208-47:
(8*5)+(7*2)+(6*6)+(5*2)+(4*0)+(3*8)+(2*4)+(1*7)=139
139 % 10 = 9
So 526208-47-9 is a valid CAS Registry Number.

526208-47-9Downstream Products

526208-47-9Relevant articles and documents

Double-Chelation-Assisted Rh-Catalyzed Intermolecular Hydroacylation between Salicylaldehydes and 1,4-Penta- or 1,5-Hexadienes

Imai, Masanori,Tanaka, Masakazu,Tanaka, Keitaro,Yamamoto, Yoichiro,Imai-Ogata, Naoko,Shimowatari, Masato,Nagumo, Shinji,Kawahara, Norio,Suemune, Hiroshi

, p. 1144 - 1150 (2007/10/03)

Intermolecular hydroacylation between salicylaldehydes 1, 26-40 and 1,4-penta- or 1,5-hexadienes 4-13 by Rh-catalyst proceeded under mild reaction conditions to give a mixture of iso- and normal-hydroacylated products 14-25, 41-55, and 57-60. In the hydroacylation reaction, chelation of both salicylaldehyde and diene to the Rh-complex plays a crucial role. The ratio of iso- and normal-hydroacylated products could be regulated by the addition of salicylic acid or amines. The effects of various Rh-complexes, solvents, and additives were examined, and the plausible mechanisms of the catalytic cycle were proposed on the basis of the deuterium-labeling salicylaldehyde experiments.

Double-chelation-assisted Rh-catalyzed intermolecular hydroacylation

Tanaka, Masakazu,Imai, Masanori,Yamamoto, Yoichiro,Tanaka, Keitaro,Shimowatari, Masato,Nagumo, Shinji,Kawahara, Norio,Suemune, Hiroshi

, p. 1365 - 1367 (2007/10/03)

(Matrix presented) Rh-Catalyzed intermolecular hydroacylation between salicylaldehydes and 1,5-hexadienes proceeded under remarkably mild reaction conditions to afford a mixture of iso- and normal-hydroacylated products in good yields. The experiments using deuterated salicylaldehyde-d revealed that "double chelation" of salicylaldehyde and 1,5-hexadiene to Rh-complex played vital roles in the catalytic cycle of intermolecular hydroacylation.

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