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CAS

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14289-61-3

1-benzyloxy-1-phenylprop-2-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 14289-61-3 Structure

  • Basic information

    1. Product Name: 1-benzyloxy-1-phenylprop-2-ene
    2. Synonyms: 1-benzyloxy-1-phenylprop-2-ene
    3. CAS NO:14289-61-3
    4. Molecular Formula:
    5. Molecular Weight: 224.302
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14289-61-3.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: 1-benzyloxy-1-phenylprop-2-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyloxy-1-phenylprop-2-ene(14289-61-3)
    11. EPA Substance Registry System: 1-benzyloxy-1-phenylprop-2-ene(14289-61-3)

  • 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: 14289-61-3(Hazardous Substances Data)

14289-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14289-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,8 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14289-61:
(7*1)+(6*4)+(5*2)+(4*8)+(3*9)+(2*6)+(1*1)=113
113 % 10 = 3
So 14289-61-3 is a valid CAS Registry Number.

14289-61-3Relevant articles and documents

Rhodium-Catalyzed Enantioselective Intermolecular Hydroalkoxylation of Allenes and Alkynes with Alcohols: Synthesis of Branched Allylic Ethers

Liu, Zi,Breit, Bernhard

supporting information, p. 8440 - 8443 (2016/07/19)

Regio- and enantioselective additions of alcohols to either terminal allenes or internal alkynes provides access to allylic ethers by using a RhI/diphenyl phosphate catalytic system. This method provides an atom-economic way to obtain chiral aliphatic and aryl allylic ethers in moderate to good yield with good to excellent enantioselectivities.

Organoselenium-catalyzed, hydroxy-controlled regio- and stereoselective amination of terminal alkenes: Efficient synthesis of 3-amino allylic alcohols

Deng, Zhimin,Wei, Jialiang,Liao, Lihao,Huang, Haiyan,Zhao, Xiaodan

supporting information, p. 1834 - 1837 (2015/04/27)

An efficient route to prepare 3-amino allylic alcohols in excellent regio- and stereoselectivity in the presence of bases by orangoselenium catalysis has been developed. In the absence of bases α,β-unsaturated aldehydes were formed in up to 97% yield. Control experiments reveal that the hydroxy group is crucial for the direct amination.

Synthesis of N-protected allylic amines from allyl ethers

Kim, Ji Duck,Lee, Min Hee,Han, Gyoonhee,Park, Hyunju,Zee, Ok Pyo,Jung, Young Hoon

, p. 8257 - 8266 (2007/10/03)

A synthetic method for N-protected allylic amines from allyl ethers using chlorosulfonyl isocyanate (CSI) is presented. The reaction of 4-phenylbut-2-enyl methyl ether (1i) with CSI afforded methyl N-(1-benzylallyl)carbamate (2i) and methyl N-(4-phenylbut

[2,3]-Wittig rearrangement initiated by 1,5-hydrogen atom transfer from an o-iodophenyl group on the α-carbon of allylic ethers by reduction with SmI2

Kunishima, Munetaka,Hioki, Kazuhito,Nakata, Daisuke,Nogawa, Shigenobu,Tani, Shohei

, p. 683 - 684 (2007/10/03)

Intramolecular 1,5-hydrogen atom transfer of an aryl radical generated by reduction of an o-iodophenyl group on the allylic position of allyl ethers by SmI2 regioselectively generates α-allyloxy carbanions, which undergo [2,3]-Wittig rearrangem

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