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3-(4-methylphenyl)but-3-en-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 57132-22-6 Structure
  • Basic information

    1. Product Name: 3-(4-methylphenyl)but-3-en-2-ol
    2. Synonyms: 3-(4-methylphenyl)but-3-en-2-ol
    3. CAS NO:57132-22-6
    4. Molecular Formula:
    5. Molecular Weight: 162.232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 57132-22-6.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: 3-(4-methylphenyl)but-3-en-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-methylphenyl)but-3-en-2-ol(57132-22-6)
    11. EPA Substance Registry System: 3-(4-methylphenyl)but-3-en-2-ol(57132-22-6)
  • 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: 57132-22-6(Hazardous Substances Data)

57132-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57132-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,3 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57132-22:
(7*5)+(6*7)+(5*1)+(4*3)+(3*2)+(2*2)+(1*2)=106
106 % 10 = 6
So 57132-22-6 is a valid CAS Registry Number.

57132-22-6Relevant articles and documents

Enantioselective Bromolactonization of Trisubstituted Olefinic Acids Catalyzed by Chiral Pyridyl Phosphoramides

Nishikawa, Yasuhiro,Hamamoto, Yuhta,Satoh, Rika,Akada, Naho,Kajita, Shuhei,Nomoto, Marina,Miyata, Megumi,Nakamura, Madoka,Matsubara, Chinatsu,Hara, Osamu

, p. 18880 - 18885 (2018/12/04)

Enantioselective bromolactonization of trisubstituted olefinic acids producing synthetically useful chiral lactones with two contiguous asymmetric centers has remained mainly unexplored except for the 6-exo cyclization mode. In this work, the 5-exo- and 6

Regioselective aerobic oxidative Heck reactions with electronically unbiased alkenes: Efficient access to α-alkyl vinylarenes

Zheng, Changwu,Stahl, Shannon S.

supporting information, p. 12771 - 12774 (2015/08/18)

Branched-selective oxidative Heck coupling reactions have been developed between arylboronic acids and electronically unbiased terminal alkenes. The reactions exhibit high catalyst-controlled regioselectivity favoring the less common branched isomer. The reactions employ a catalyst composed of Pd(TFA)2/dmphen (TFA = trifluoroacetate, dmphen = 2,9-dimethyl-1,10-phenanthroline) and proceed efficiently at 45-60 °C under 1 atm of O2 without requiring other additives. A broad array of functional groups, including aryl halide, allyl silane and carboxylic acids are tolerated.

Nonenzymatic kinetic resolution of α-aryl substituted allylic alcohols catalyzed by acyl transfer catalyst Np-PIQ

Jiang, Shan-Shan,Gu, Bo-Qi,Zhu, Ming-Yu,Yu, Xingxin,Deng, Wei-Ping

, p. 1187 - 1191 (2015/02/19)

Chiral α-aryl substituted allylic alcohols are important versatile synthetic intermediates. We report here an effective nonenzymatic kinetic resolution of racemic α-aryl substituted allylic alcohols by introducing different aryl groups with acyl transfer

C2-symmetric cyclic selenium-catalyzed enantioselective bromoaminocyclization

Chen, Feng,Tan, Chong Kiat,Yeung, Ying-Yeung

supporting information, p. 1232 - 1235 (2013/03/28)

A catalytic asymmetric bromocyclization of trisubstituted olefinic amides that uses a C2-symmetric mannitol-derived cyclic selenium catalyst and a stoichiometric amount of N-bromophthalimide is reported. The resulting enantioenriched pyrrolidine products, which contain two stereogenic centers, can undergo rearrangement to yield 2,3-disubstituted piperidines with excellent diastereoselectivity and enantiospecificity.

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