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81112-84-7

5-(1-hydroxy-3-phenylpropyl)furan-2(5H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81112-84-7 Structure

  • Basic information

    1. Product Name: 5-(1-hydroxy-3-phenylpropyl)furan-2(5H)-one
    2. Synonyms: 5-(1-hydroxy-3-phenylpropyl)furan-2(5H)-one
    3. CAS NO:81112-84-7
    4. Molecular Formula:
    5. Molecular Weight: 218.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81112-84-7.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: 5-(1-hydroxy-3-phenylpropyl)furan-2(5H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(1-hydroxy-3-phenylpropyl)furan-2(5H)-one(81112-84-7)
    11. EPA Substance Registry System: 5-(1-hydroxy-3-phenylpropyl)furan-2(5H)-one(81112-84-7)

  • 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: 81112-84-7(Hazardous Substances Data)

81112-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81112-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,1 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81112-84:
(7*8)+(6*1)+(5*1)+(4*1)+(3*2)+(2*8)+(1*4)=97
97 % 10 = 7
So 81112-84-7 is a valid CAS Registry Number.

81112-84-7Relevant articles and documents

Asymmetric vinylogous aldol reaction of silyloxy furans with a chiral organic salt

Singh, Ravi P.,Foxman, Bruce M.,Deng, Li

supporting information; experimental part, p. 9558 - 9560 (2010/08/20)

Despite their synthetic significance there is a general lack of asymmetric vinylogous aldol reactions that tolerate variations of both the silyloxy furans and aldehydes. We have developed a new chiral organic catalyst based on a carboxylate-ammonium salt prepared from a thiourea-amine and a carboxylic acid. This new catalyst enabled us to develop an efficient asymmetric vinylogous aldol reaction of unprecedented scope with respect to both 2-trimethylsilyloxy furans and aldehydes.

Enantioselective addition of 2-(trimethylsilyloxy)furan to aldehydes using Cr(salen) as catalyst. Effect of water on enantioselectivity

Matsuoka, Yuko,Irie, Ryo,Katsuki, Tsutomu

, p. 584 - 585 (2007/10/03)

Cationic (R,R)-Cr(salen) complex 2 was found to catalyze enantioselective addition of 2-(trimethylsilyloxy)furan to aldehydes to give 5-substituted butenolides, though diastereoselectivity was only modest. The presence of a small amount of water is essential for achieving high enantioselectivity.

SYNTHESIS OF 4-YLIDENEBUTENOLIDES FROM 2-TRIMETHYLSILOXYFURAN

Asaoka, Morio,Yanagida, Noboru,Ishibashi, Keiji,Takei, Hisashi

, p. 4269 - 4270 (2007/10/02)

Dehydration or dealkoxylation of the reaction products of various aldehydes, ketones, and acetals with 2-trimethylsiloxyfuran gave corresponding 4-ylidenebutenolides in good to high overall yields.

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