Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1391852-80-4

5-(chloromethyl)-1-phenylhex-5-en-2-yn-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1391852-80-4 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1391852-80-4 Structure

  • Basic information

    1. Product Name: 5-(chloromethyl)-1-phenylhex-5-en-2-yn-1-ol
    2. Synonyms:
    3. CAS NO:1391852-80-4
    4. Molecular Formula:
    5. Molecular Weight: 220.699
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1391852-80-4.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-(chloromethyl)-1-phenylhex-5-en-2-yn-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(chloromethyl)-1-phenylhex-5-en-2-yn-1-ol(1391852-80-4)
    11. EPA Substance Registry System: 5-(chloromethyl)-1-phenylhex-5-en-2-yn-1-ol(1391852-80-4)

  • 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: 1391852-80-4(Hazardous Substances Data)

1391852-80-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1391852-80-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,1,8,5 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1391852-80:
(9*1)+(8*3)+(7*9)+(6*1)+(5*8)+(4*5)+(3*2)+(2*8)+(1*0)=184
184 % 10 = 4
So 1391852-80-4 is a valid CAS Registry Number.

1391852-80-4Relevant articles and documents

Gold-Catalyzed Dehydrogenative Cycloisomerization of 1,4-Enyne Esters to 3,5-Disubstituted Phenol Derivatives

Chen, Cuili,Chen, Xianxiao,Zhang, Xiaoxiang,Wang, Shifa,Rao, Weidong,Chan, Philip Wai Hong

, p. 4359 - 4368 (2017/12/26)

A method to prepare synthetically important 3,5-disubstituted phenol derivatives that relies on the sequential gold(I)-catalyzed dehydrogenative cycloisomerization of 1,4-enyne esters in the presence of 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) or N-fluorobenzenesulfonimide (NFSI) is described. The synthetic versatility of the methodology was exemplified by a gram-scale reaction of one example, the ease to realize subsequent functional transformations of an adduct, and the application of the method to the synthesis of the bioactive molecule LUF5771. (Figure presented.).

Bronsted acid catalyzed cycloisomerizations of 5,2-enyne-1-ones: Highly regioselective synthesis of 2,3-dihydro-4H-pyran-4-ones

Yang, Fang,Ji, Ke-Gong,Zhao, Shu-Chun,Ali, Shaukat,Ye, Yu-Ying,Liu, Xue-Yuan,Liang, Yong-Min

supporting information; experimental part, p. 6470 - 6474 (2012/06/15)

Dual-action catalyst: A Bronsted acid catalyzed regioselective cycloisomerization was found to be highly effective for the preparation of structurally diverse 2,3-dihydro-4H-pyran-4-ones in a 6-exo-trig manner from the corresponding 5,2-enyne-1-ones. In t

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1391852-80-4