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CAS

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148761-93-7

1-(2-iodophenyl)-2-propen-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148761-93-7 Structure

  • Basic information

    1. Product Name: 1-(2-iodophenyl)-2-propen-1-ol
    2. Synonyms: 1-(2-iodophenyl)-2-propen-1-ol
    3. CAS NO:148761-93-7
    4. Molecular Formula:
    5. Molecular Weight: 260.074
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148761-93-7.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: 1-(2-iodophenyl)-2-propen-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-iodophenyl)-2-propen-1-ol(148761-93-7)
    11. EPA Substance Registry System: 1-(2-iodophenyl)-2-propen-1-ol(148761-93-7)

  • 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: 148761-93-7(Hazardous Substances Data)

148761-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148761-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,7,6 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 148761-93:
(8*1)+(7*4)+(6*8)+(5*7)+(4*6)+(3*1)+(2*9)+(1*3)=167
167 % 10 = 7
So 148761-93-7 is a valid CAS Registry Number.

148761-93-7Relevant articles and documents

[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 (1999)

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

Regio- and enantioselective synthesis of chiral pyrimidine acyclic nucleosides via rhodium-catalyzed asymmetric allylation of pyrimidines

Liang, Lei,Xie, Ming-Sheng,Qin, Tao,Zhu, Man,Qu, Gui-Rong,Guo, Ha-Ming

supporting information, p. 5212 - 5215 (2017/11/06)

A direct route to branched N-allylpyrimidine analogues is herein reported via the highly regio- and enantioselective asymmetric allylation of pyrimidines with racemic allylic carbonates. With [Rh(COD)Cl]2/chiral diphosphine as the catalyst, a r

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