Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1489-57-2

Post Buying Request

1489-57-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1489-57-2 Usage

Preparation

By dehalogenation of 1,2-dibromo-1-methyl cyclohexane with sodium ethoxide; purified by distillation over metallic sodium.

Check Digit Verification of cas no

The CAS Registry Mumber 1489-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1489-57:
(6*1)+(5*4)+(4*8)+(3*9)+(2*5)+(1*7)=102
102 % 10 = 2
So 1489-57-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H10/c1-7-5-3-2-4-6-7/h3,5-6H,2,4H2,1H3

1489-57-2Relevant articles and documents

Moss,Ho

, p. 3397,3398 (1976)

(Guanidine)copper Complex-Catalyzed Enantioselective Dynamic Kinetic Allylic Alkynylation under Biphasic Condition

Cui, Xi-Yang,Ge, Yicen,Tan, Siu Min,Jiang, Huan,Tan, Davin,Lu, Yunpeng,Lee, Richmond,Tan, Choon-Hong

supporting information, p. 8448 - 8455 (2018/06/22)

Highly enantioselective allylic alkynylation of racemic bromides under biphasic condition is furnished in this report. This approach employs functionalized terminal alkynes as pro-nucleophiles and provides 6- and 7-membered cyclic 1,4-enynes with high yields and excellent enantioselectivities (up to 96% ee) under mild conditions. Enantioretentive derivatizations highlight the synthetic utility of this transformation. Cold-spray ionization mass spectrometry (CSI-MS) and X-ray crystallography were used to identify some catalytic intermediates, which include guanidinium cuprate ion pairs and a copper-alkynide complex. A linear correlation between the enantiopurity of the catalyst and reaction product indicates the presence of a copper complex bearing a single guanidine ligand at the enantio-determining step. Further experimental and computational studies supported that the alkynylation of allylic bromide underwent an anti-SN2′ pathway catalyzed by nucleophilic cuprate species. Moreover, metal-assisted racemization of allylic bromide allowed the reaction to proceed in a dynamic kinetic fashion to afford the major enantiomer in high yield.

A Versatile Route to 2-Substituted Cyclic 1,3-Dienes via a Copper(I)-Catalyzed Cross-Coupling Reaction of Dienyl Triflates with Grignard Reagents

Karlstroem, A. Sofia E.,Roenn, Magnus,Thorarensen, Atli,Baeckvall, Jan-E.

, p. 2517 - 2522 (2007/10/03)

A general synthesis of 2-substituted cyclic 1,3-dienes in two steps from α,β-unsaturated ketones has been developed. Formation of a dien-2-yl triflate followed by a copper(I)-catalyzed cross-coupling reaction with a Grignard reagent gives 2-substituted dienes in fair to excellent yields. Alkyl, aryl, and allyl Grignard reagents can be used.

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 1489-57-2